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Version 1. F1000Res. 2016; 5: F1000 Faculty Rev-1497.
Published online 2016 June 24. doi:  10.12688/f1000research.8584.1
PMCID: PMC4926734

Recent advances in understanding ichthyosis pathogenesis

Abstract

The ichthyoses, also known as disorders of keratinization (DOK), encompass a heterogeneous group of skin diseases linked by the common finding of abnormal barrier function, which initiates a default compensatory pathway of hyperproliferation, resulting in the characteristic clinical manifestation of localized and/or generalized scaling. Additional cutaneous findings frequently seen in ichthyoses include generalized xerosis, erythroderma, palmoplantar keratoderma, hypohydrosis, and recurrent infections. In 2009, the Ichthyosis Consensus Conference established a classification consensus for DOK based on pathophysiology, clinical manifestations, and mode of inheritance. This nomenclature system divides DOK into two main groups: nonsyndromic forms, with clinical findings limited to the skin, and syndromic forms, with involvement of additional organ systems. Advances in next-generation sequencing technology have allowed for more rapid and cost-effective genetic analysis, leading to the identification of novel, rare mutations that cause DOK, many of which represent phenotypic expansion. This review focuses on new findings in syndromic and nonsyndromic ichthyoses, with emphasis on novel genetic discoveries that provide insight into disease pathogenesis.

Keywords: ichthyosis, keratinization, hyperproliferation, pathogenesis

Introduction

The ichthyoses encompass a heterogeneous group of skin diseases linked by the common finding of abnormal barrier function, which leads to increased transepidermal water loss and compensatory hyperproliferation. The unifying phenotypic feature of the ichthyoses is localized and/or generalized scaling. Other clinical manifestations can include erythroderma (confluent red skin), palmoplantar keratoderma (thickening of the palms and soles), hypohydrosis (diminished sweating), and recurrent infections.

Although ichthyoses are primarily inherited disorders with onset at or shortly after birth, rare acquired forms have been reported in the setting of malignancy, nutritional deficiency, and autoimmune or infectious disease. Mutations in over 50 genes have been reported to cause ichthyoses, and these affect a host of cellular functions including DNA repair, lipid biosynthesis, adhesion, and desquamation as well as other pathways 1. Despite myriad pathways for pathogenesis, each features disrupted barrier function.

Epidermal barrier function is maintained by a regular pattern of epidermal renewal in which keratinocytes, the primary cell type of the skin, arise from a renewing stem cell pool and undergo a tightly regulated pattern of differentiation as they transit from the innermost stratum basale to the outermost stratum corneum, where they are ultimately sloughed off. This differentiation program is marked by site-specific expression of proteins and, in the suprabasal layers, the production of components necessary for the generation of the lipid barrier.

In the process of differentiation, keratins—intermediate filaments that are responsible for the structural integrity of keratinocytes—are among the first proteins to be expressed in a tightly regulated manner, with keratin 5 and 14 expressed in the basal layer and keratin 1 and 10 expressed in the suprabasal layers. In the stratum spinosum, the second innermost layer of the epidermis, components of the lipid barrier (phospholipids, cholesterol, sphingomyelin, and glucosylceramides) are packaged into lamellar bodies, which are specialized organelles that house the building blocks of the lipid barrier as well as enzymes essential to the processing of lipid barrier precursors. At the transition from the stratum granulosum—the third layer of the epidermis—to the stratum corneum, the contents of lamellar bodies are extruded into the intercellular space to form protective lipid sheets that are responsible for the skin’s hydrophobic barrier 2, 3 ( Figure 1).

Figure 1.
Epidermal structure

This overall process of differentiation results in the formation of a robust barrier in the stratum corneum, composed of keratinocytes (the individual bricks of the barrier) and inter-keratinocyte lipids (the mortar) 4. Mutations in proteins essential to the formation of this barrier (i.e. keratins and enzymes involved in lipid synthesis) lead to the disruption of barrier integrity, resulting in ichthyosis.

Inherited ichthyoses exhibit marked genetic and phenotypic heterogeneity, and advances in next-generation sequencing technology have allowed for more rapid and cost-effective genetic analysis, leading to the identification of novel, rare mutations that cause DOK. Clear large-scale genotype-phenotype correlations have been difficult to establish, as mutations in the same gene can present with widely divergent phenotypes, even within kindreds bearing the same disease-causing mutation.

In 2009, the Ichthyosis Consensus Conference established a consensus classification for DOK based on pathophysiology, clinical manifestations, and mode of inheritance 1. This nomenclature system divides DOK into two main groups: 1) nonsyndromic forms, with clinical findings limited to the skin, and 2) syndromic forms, with involvement of other organ systems.

Nonsyndromic ichthyoses

Common ichthyoses

Ichthyosis vulgaris (IV) and X-linked recessive ichthyosis (XLRI) are classified as the “common ichthyoses”, given their high prevalence. IV is the most common form of nonsyndromic inherited ichthyosis, with an estimated incidence of 1 in 250 births 5. Typically, IV is a phenotypically mild form of ichthyosis. Clinical findings usually appear at around 2 months of age and include generalized xerosis and fine white to gray scale that is most prominent on the abdomen, chest, and extensor surfaces of the extremities. Keratosis pilaris and hyper-linearity of the palms and soles are also frequently associated with IV.

IV is caused by autosomal dominant mutations in the filaggrin gene ( FLG), which plays an essential role in epidermal differentiation and formation of the skin barrier 6, 7. An autosomal semidominant mode of inheritance has also been described, meaning that while individuals with heterozygous mutations have a mild phenotype, those with homozygous or compound heterozygous mutations can display more severe forms of ichthyosis 6.

Patients with IV are at increased risk for atopic dermatitis, asthma, and allergies 8, 9. This increased risk is likely due to disruption of barrier function, which may allow for greater penetration of the epidermis by potential allergens 8.

XLRI is the second most common form of inherited ichthyosis, with a prevalence of 1:2000 to 1:6000 in males 10. Clinical findings in XLRI are frequently indistinguishable from IV. Manifestations usually first appear in the neonatal period as generalized desquamation and xerosis and progress to fine scaling of the trunk and extremities in infancy. Over time, patients develop brownish, polygonal, plate-like scale that is tightly adherent to the skin. XLRI is caused by mutations in the STS gene, encoding steroid sulfatase, on the X chromosome 11.

Autosomal recessive congenital ichthyosis

Autosomal recessive congenital ichthyosis (ARCI) is a genetically and phenotypically heterogeneous group of disorders that includes harlequin ichthyosis (HI), lamellar ichthyosis (LI), and congenital ichthyosiform erythroderma (CIE). The incidence of ARCI has been approximated at 1 in 200,000 births 12.

HI is caused by loss-of-function mutations in ABCA12, which encodes an ATP-binding cassette (ABC) transporter. ABCA12 is necessary for lipid transport into lamellar granules and is central to the process of cornification and lipid barrier formation 13. Interestingly, while homozygous loss-of-function mutations in ABCA12 lead to HI, missense mutations in ABCA12 result in milder phenotypes on the LI/CIE spectrum 14. Neonates with HI present with thick, armor-like scale with severe ectropion (eversion of the eyelids), eclabium (eversion of the lips), and flattening of the ears. Some patients with HI die during the neonatal period, but survival has been shown to improve with progress in neonatal intensive care and early treatment with systemic retinoids. Rajpopat et al. showed that 83% of HI patients treated with oral retinoids survived compared to 24% of untreated patients 15.

LI and CIE represent a spectrum of disorders caused by mutations in one of nine genes: TGM1, NIPAL4/ICHTHYIN, ALOX12B, ALOXE3, CYP4F22, ABCA12, PNPLA1, CERS3, and LIPN 16. Mutations in TGM1 are the most common and account for approximately 32% of heritability of ARCI 17. Fisher et al. found that mutations in the six most common genes ( TGM1, NIPAL4, ALOX12B, CYP4F22, ALOXE3, and ABCA12) account for 78% of ARCI cases 17. Despite this, prior studies of large cohorts of patients with ARCI showed that 22-40% of patients have no mutations in known genes 17, 18, highlighting the heterogeneity of this group of disorders and the importance of continued efforts in gene discovery.

Keratinopathic ichthyosis

Keratinopathic ichthyosis is a group of disorders caused by mutations in the keratin family of genes. The major variant of keratinopathic ichthyosis is epidermolytic ichthyosis (EI). Minor variants include superficial EI (SEI), annular EI (AEI), and ichthyosis Curth-Macklin.

EI is caused by autosomal dominant mutations in the keratin 1 ( KRT1) and keratin 10 ( KRT10) genes, which play an essential role in maintaining structural integrity in suprabasal keratinocytes 19. EI is characterized by marked skin fragility, leading to generalized blister formation on a background of erythroderma. Neonates present with blistering and erythema at birth, but symptoms improve over time. Blistering becomes less frequent and is usually confined to sites of trauma in adulthood. Palmoplantar keratoderma is often associated with EI, although it is more commonly seen in patients with mutations in KRT1 than KRT10 19.

SEI, also known as ichthyosis bullosa of Siemens, is caused by mutations in KRT2 20, 21. Phenotypic manifestations are milder compared to EI and include blister formation in response to trauma and hyperkeratosis (thickening of the stratum corneum) over flexural areas.

AEI is a rare phenotypic variant of EI that was shown by Yang et al. to be caused by a unique mutation in KRT10 that replaces an alanine at residue 12 with a proline 22. It is characterized by blister formation at birth, which later progresses to the intermittent development of annular polycyclic erythematous plaques on the trunk and extremities.

Ichthyosis Curth-Macklin is another rare disorder and is caused by autosomal dominant mutations in KRT1 23, 24. It is characterized by extensive spiky or verrucous hyperkeratosis over the trunk and extensor surfaces of the extremities. It may also be associated with severe palmoplantar keratoderma. In the past 5 years, two novel distinct causative mutations in KRT1 have been identified in addition to the two mutations that were initially described 25, 26. While both EI and ichthyosis Curth-Macklin can be caused by mutations in KRT1, EI is caused by amino acid substitutions and in-frame deletions in the gene 27, while ichthyosis Curth-Macklin is caused by insertions or deletions that lead to a frameshift 2326.

Syndromic ichthyoses

In addition to cutaneous involvement, syndromic ichthyoses affect at least one other organ or system. Many causative genes have been identified for syndromic ichthyoses, including NSDHL (CHILD syndrome) 28, EBP (Conradi-Hunermann-Happle syndrome, CHILD Syndrome) 28, 29, and ALDH3A2 (Sjögren-Larsson syndrome) 30. Depending on the specific gene mutated, a wide range of organ systems can be involved, including the skeletal, nervous, endocrine, and cardiovascular systems. Many of the syndromic ichthyoses may present at birth with isolated cutaneous findings, highlighting the importance of a high degree of clinical suspicion and the usefulness of genetic analysis in the early diagnosis of these syndromic cases.

Recent advances in ichthyosis

Nonsyndromic ichthyoses

Mutations in PNPLA1 cause autosomal recessive congenital ichthyosis. In 2012, Grall et al. reported that mutations in the patatin-like phospholipase domain-containing protein 1 gene ( PNPLA1) cause ARCI in Golden Retriever dogs and humans 31. Selective inbreeding of dogs to create pure breeds leads to the propagation of not only specific desirable traits but also disease-causing alleles. The selection of these undesirable alleles results in the high prevalence of breed-specific diseases in dogs. For example, the inbreeding of Golden Retrievers has led to the high prevalence of ichthyosis within the breed. The frequency of the mutation in Golden Retrievers is estimated to be approximately 50% 31. Ichthyosis in Golden Retrievers presents with generalized scaling, with white or black scale, similar to the phenotypic manifestations of ichthyosis in humans.

Intermarriage within families and breeding approaches for purebred animals provide a unique opportunity to study the genetic basis of rare conditions. Grall et al. performed genetic analysis on 20 affected Golden Retrievers, which revealed homozygous mutations in PNPLA1 in all members of the cohort. Further studies on a human cohort of 46 consanguineous families with ARCI, who were previously found not to have mutations in known ARCI genes, revealed two distinct mutations in PNPLA1 in two different families 31.

The PNPLA family of proteins contains nine members, which play key roles in lipid metabolism 32, 33. While disease-causing mutations in other members of the family had been previously identified, mutations in PNPLA1 had not been previously implicated in any disease 3437. This finding not only expands the genetic understanding of ARCI but also highlights the essential role of PNPLA1 in lipid metabolism and maintenance of the barrier function.

Mutations in GJA1 cause erythrokeratodermia variabilis et progressiva. In 2015, Boyden et al. reported that autosomal dominant mutations in GJA1 cause erythrokeratodermia variabilis et progressiva (EKVP) 38, a rare genetic disorder characterized by transient figurate erythematous patches on a background of generalized scaling. GJA1 encodes connexin 43 (Cx43), which is present throughout the epidermis and is expressed in every tissue type 39. Connexins, also known as gap junction proteins, are classified into alpha and beta subgroups 40, encoded by GJA and GJB genes, respectively. Individual connexins form hexamers called connexons.

Connexons can serve two main functions within the plasma membrane—individual connexons can either function as hemichannels, allowing for communication between the cytoplasm and the extracellular space, or dock with connexons on neighboring cells to form gap junctions. Gap junctions are essential to intercellular communication, allowing for synchronization of metabolic and electrical activities between cells as well as the exchange of small molecules and ions. Mutations in connexin genes have been previously shown to cause a wide range of disease phenotypes, including myelin-related disease, skin disease, hearing loss, and congenital cataract 41.

While mutations in GJB3 and GJB4 have been previously shown to cause EKV/EKVP 42, 43, Boyden et al. were first to report that mutations in GJA1 can also cause the phenotype 38. Mutations in GJA1 have been previously described to cause oculodentodigital dysplasia (ODDD) 39, 44, which is a systemic disorder with limited cutaneous findings and sharply contrasts with the widespread cutaneous findings with lack of systemic symptoms seen in EKVP. Mutations in GJA1 that result in EKVP lead to mislocalization of Cx43 38, while mutations resulting in ODDD lead to functionally impaired gap junctions that show a normal pattern of localization 45. This finding expands the genetic understanding of EKVP and provides insight into its molecular mechanism.

Mutations in CARD14 cause pityriasis rubra pilaris. Pityriasis rubra pilaris (PRP) is a papulosquamous disorder that is characterized by well-demarcated salmon-colored plaques with fine scale, palmoplantar keratoderma, and follicular hyperkeratosis (excessive accumulation of keratin in hair follicles) that presents shortly after birth or can be acquired later in life, typically in the fourth or fifth decade. Although phenotypic features of PRP overlap with psoriasis, the two can be distinguished based on distinct clinical and histopathological factors 4649. There is much debate over the pathogenesis of PRP: infectious, inflammatory, and vitamin A-associated etiologies have been proposed 46, 5052. A small fraction of PRP cases (less than 5%) are familial and are inherited in an autosomal dominant fashion 46, 53, 54.

In 2012, Fuchs-Telem et al. studied four unrelated families with familial PRP and identified three distinct mutations in caspase recruitment domain family member 14 ( CARD14) 55. CARD14 is a known modulator of nuclear factor kappa B (NF-κB), which plays an important role in inflammatory pathways 56, 57. Fuchs-Telem et al. showed that NF-κB signaling is activated in PRP-affected skin and suggested that this inflammatory upregulation may play a role in the pathogenesis of familial PRP. Interestingly, causative mutations in CARD14 were previously identified in familial psoriasis, and enhanced NF-κB signaling was also identified as a possible pathogenic factor 58. Taken together, these findings indicate that in addition to similarities in phenotypic features, familial PRP and familial psoriasis may share a common pathophysiology. Given the overall poor response to current treatments for PRP, this finding may allow for new therapeutic approaches that are aimed at modulating the immune response.

Specific mutations in TGM1 cause bathing-suit ichthyosis. As discussed above, ARCI encompasses a wide range of phenotypes, including LI, CIE, and HI. The most common underlying gene defect is the tranglutaminase-1 gene ( TGM1), which accounts for approximately 30% of heritability of ARCI 17.

Bathing-suit ichthyosis (BSI) is a rare variant of ARCI and is distinguished from the other forms of ARCI by restriction of scaling to the trunk, with sparing of the central face, buttocks, and limbs. All cases of BSI published to date have been caused by mutations in TGM1, although mutations in TGM1 more commonly cause generalized ARCI 5961. In 2006, Oji et al. showed that the specific TGM1 mutations that cause BSI may lead to temperature-dependent activity of transglutaminase, with marked decrease in enzyme function at higher temperatures 61. This may account for the differential scaling observed in BSI, with greater disease manifestation at sites with relatively higher temperature, such as the trunk. More recently, several studies have identified additional mutations in TGM1 that contribute to BSI 6264, furthering the genetic understanding of this rare type of ichthyosis.

Syndromic ichthyoses

Mutations in DSP cause erythrokeratodermia-cardiomyopathy syndrome. In 2016, Boyden et al. identified a novel cardio-cutaneous disorder known as erythrokeratodermia-cardiomyopathy (EKC) syndrome. Early clinical findings include generalized erythrokeratodermia, recurrent infections, and failure to thrive as well as wiry or absent hair, dental enamel defects, absence of secondary teeth, and nail dystrophy. A hallmark of EKC is initially asymptomatic, rapidly progressive, potentially fatal cardiomyopathy, which was found in all three patients with EKC published in the literature to date 65.

EKC is caused by mutations in DSP, which encodes desmoplakin, a primary component of desmosomes 65. Desmosomes are intercellular adhesion junctions that are most abundant in the epidermis and the heart. DSP has been previously implicated in several disorders, including diseases with isolated cardiac manifestations and cardio-cutaneous syndromes. Examples of disorders caused by mutations in DSP include striate palmoplantar keratoderma, smooth palmoplantar keratoderma with woolly hair, Carvajal syndrome (dilated cardiomyopathy with woolly hair and keratoderma), and arrhythmogenic cardiomyopathy 6670. However, EKC syndrome represents a distinct clinical phenotype and is the only disorder caused by mutations in DSP to present with erythrokeratodermia 65.

Although EKC syndrome is a distinct entity based on specific clinical features and unique pathobiology, its initial clinical manifestation can appear very similar to CIE, which would not prompt any further cardiac evaluation. The description of this novel syndrome emphasizes the critical, potentially life-saving importance of genetic diagnosis in patients with ichthyosis.

Mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia. In 2011, Aldamesh et al. identified a novel neuro-ichthyotic disease caused by autosomal recessive mutations in ELOVL4 and characterized by ichthyosis, mental retardation, seizures, and spastic quadriplegia 71. These phenotypic manifestations are similar to those of Sjögren-Larrson syndrome, a syndromic ichthyosis caused by mutations in fatty aldehyde dehydrogenase ( ALDH3A2) 30, but the neurologic findings in this newly described disorder are more severe 71.

ELOVL4 is a fatty acid elongase and plays a crucial role in the synthetic pathway of very-long-chain fatty acids (VLCFAs) 72. VLCFAs have a wide range of functions, including cell signaling and maintenance of the epidermal barrier 7378. Heterozygous mutations in ELOVL4 had been previously reported to cause macular degeneration 79, but Aldamesh et al. were first to report the involvement of homozygous ELOVL4 mutations in an ichthyosis syndrome, with both cutaneous and neurologic findings. In addition to identifying a novel syndromic ichthyosis, this finding highlights the importance of VLCFAs in both brain development and maintenance of epidermal barrier function. It also suggests the use of VLCFA replacement therapy as a possible therapeutic option for the treatment of patients with this disorder.

Notes

[version 1; referees: 2 approved]

Funding Statement

The author(s) declared that no grants were involved in supporting this work.

Notes

Editorial Note on the Review Process

F1000 Faculty Reviews are commissioned from members of the prestigious F1000 Faculty and are edited as a service to readers. In order to make these reviews as comprehensive and accessible as possible, the referees provide input before publication and only the final, revised version is published. The referees who approved the final version are listed with their names and affiliations but without their reports on earlier versions (any comments will already have been addressed in the published version).

The referees who approved this article are:

  • Anna Bruckner, Department of Dermatology, University of Colorado, Aurora, CO, USA
    No competing interests were disclosed.
  • Masashi Akiyama, Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    No competing interests were disclosed.

References

1. Oji V, Tadini G, Akiyama M, et al. : Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. J Am Acad Dermatol. 2010;63(4):607–41. 10.1016/j.jaad.2009.11.020 [PubMed] [Cross Ref]
2. Feingold KR.: The outer frontier: the importance of lipid metabolism in the skin. J Lipid Res. 2009;50(Suppl):S417–22. 10.1194/jlr.R800039-JLR200 [PMC free article] [PubMed] [Cross Ref]
3. Madison KC.: Barrier function of the skin: "la raison d'être" of the epidermis. J Invest Dermatol. 2003;121(2):231–41. 10.1046/j.1523-1747.2003.12359.x [PubMed] [Cross Ref]
4. Nemes Z, Steinert PM.: Bricks and mortar of the epidermal barrier. Exp Mol Med. 1999;31(1):5–19. 10.1038/emm.1999.2 [PubMed] [Cross Ref]
5. Wells RS, Kerr CB.: Clinical features of autosomal dominant and sex-linked ichthyosis in an English population. Br Med J. 1966;1(5493):947–50. 10.1136/bmj.1.5493.947 [PMC free article] [PubMed] [Cross Ref]
6. Smith FJ, Irvine AD, Terron-Kwiatkowski A, et al. : Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris. Nat Genet. 2006;38(3):337–42. 10.1038/ng1743 [PubMed] [Cross Ref]
7. Thyssen JP, Godoy-Gijon E, Elias PM.: Ichthyosis vulgaris: the filaggrin mutation disease. Br J Dermatol. 2013;168(6):1155–66. 10.1111/bjd.12219 [PubMed] [Cross Ref]
8. Osawa R, Akiyama M, Shimizu H.: Filaggrin gene defects and the risk of developing allergic disorders. Allergol Int. 2011;60(1):1–9. 10.2332/allergolint.10-RAI-0270 [PubMed] [Cross Ref]
9. Sandilands A, Terron-Kwiatkowski A, Hull PR, et al. : Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema. Nat Genet. 2007;39(5):650–4. 10.1038/ng2020 [PubMed] [Cross Ref]
10. Lykkesfeldt G, Nielsen MD, Lykkesfeldt AE.: Placental steroid sulfatase deficiency: biochemical diagnosis and clinical review. Obstet Gynecol. 1984;64(1):49–54. [PubMed]
11. del Refugio Rivera Vega M, Murillo-Vilches MR, Toral-Lopez J, et al. : X-linked ichthyosis in a patient with a novel nonsense mutation in the STS gene. J Dermatol Sci. 2015;80(2):160–2. 10.1016/j.jdermsci.2015.09.004 [PubMed] [Cross Ref]
12. Richard G, Bale SJ.: Autosomal Recessive Congenital Ichthyosis. In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, et al., editors. GeneReviews(R). Seattle (WA);1993.
13. Mitsutake S, Suzuki C, Akiyama M, et al. : ABCA12 dysfunction causes a disorder in glucosylceramide accumulation during keratinocyte differentiation. J Dermatol Sci. 2010;60(2):128–9. 10.1016/j.jdermsci.2010.08.012 [PubMed] [Cross Ref]
14. Akiyama M.: ABCA12 mutations and autosomal recessive congenital ichthyosis: a review of genotype/phenotype correlations and of pathogenetic concepts. Hum Mutat. 2010;31(10):1090–6. 10.1002/humu.21326 [PubMed] [Cross Ref]
15. Rajpopat S, Moss C, Mellerio J, et al. : Harlequin ichthyosis: a review of clinical and molecular findings in 45 cases. Arch Dermatol. 2011;147(6):681–6. 10.1001/archdermatol.2011.9 [PubMed] [Cross Ref]
16. Takeichi T, Akiyama M.: Inherited ichthyosis: Non-syndromic forms. J Dermatol. 2016;43(3):242–51. 10.1111/1346-8138.13243 [PubMed] [Cross Ref]
17. Fischer J.: Autosomal recessive congenital ichthyosis. J Invest Dermatol. 2009;129(6):1319–21. 10.1038/jid.2009.57 [PubMed] [Cross Ref]
18. Eckl KM, de Juanes S, Kurtenbach J, et al. : Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B. J Invest Dermatol. 2009;129(6):1421–8. 10.1038/jid.2008.409 [PubMed] [Cross Ref]
19. Arin MJ, Oji V, Emmert S, et al. : Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis. Br J Dermatol. 2011;164(2):442–7. 10.1111/j.1365-2133.2010.10096.x [PubMed] [Cross Ref]
20. Cervantes T, Pham C, Browning JC.: Superficial epidermolytic ichthyosis: a report of two families. Pediatr Dermatol. 2013;30(4):469–72. 10.1111/j.1525-1470.2012.01750.x [PubMed] [Cross Ref]
21. Rothnagel JA, Traupe H, Wojcik S, et al. : Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens. Nat Genet. 1994;7(4):485–90. 10.1038/ng0894-485 [PubMed] [Cross Ref]
22. Yang JM, Yoneda K, Morita E, et al. : An alanine to proline mutation in the 1A rod domain of the keratin 10 chain in epidermolytic hyperkeratosis. J Invest Dermatol. 1997;109(5):692–4. 10.1111/1523-1747.ep12338320 [PubMed] [Cross Ref]
23. Richardson ES, Lee JB, Hyde PH, et al. : A novel mutation and large size polymorphism affecting the V2 domain of keratin 1 in an African-American family with severe, diffuse palmoplantar keratoderma of the ichthyosis hystrix Curth-Macklin type. J Invest Dermatol. 2006;126(1):79–84. 10.1038/sj.jid.5700025 [PubMed] [Cross Ref]
24. Sprecher E, Ishida-Yamamoto A, Becker OM, et al. : Evidence for novel functions of the keratin tail emerging from a mutation causing ichthyosis hystrix. J Invest Dermatol. 2001;116(4):511–9. 10.1046/j.1523-1747.2001.01292.x [PubMed] [Cross Ref]
25. Fonseca DJ, Rojas RF, Vergara JI, et al. : A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene. Br J Dermatol. 2013;168(2):456–8. 10.1111/j.1365-2133.2012.11181.x [PubMed] [Cross Ref]
26. Kubo Y, Urano Y, Matsuda R, et al. : Ichthyosis hystrix, Curth-Macklin type: a new sporadic case with a novel mutation of keratin 1. Arch Dermatol. 2011;147(8):999–1001. 10.1001/archdermatol.2011.217 [PubMed] [Cross Ref]
27. Mirza H, Kumar A, Craiglow BG, et al. : Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis. J Invest Dermatol. 2015;135(12):3041–50. 10.1038/jid.2015.284 [PubMed] [Cross Ref]
28. Lai-Cheong JE, Elias PM, Paller AS.: Pathogenesis-based therapies in ichthyoses. Dermatol Ther. 2013;26(1):46–54. 10.1111/j.1529-8019.2012.01528.x [PMC free article] [PubMed] [Cross Ref]
29. Canueto J, Girós M, Ciria S, et al. : Clinical, molecular and biochemical characterization of nine Spanish families with Conradi-Hünermann-Happle syndrome: new insights into X-linked dominant chondrodysplasia punctata with a comprehensive review of the literature. Br J Dermatol. 2012;166(4):830–8. 10.1111/j.1365-2133.2011.10756.x [PubMed] [Cross Ref]
30. Gaboon NE, Jelani M, Almramhi MM, et al. : Case of Sjögren-Larsson syndrome with a large deletion in the ALDH3A2 gene confirmed by single nucleotide polymorphism array analysis. J Dermatol. 2015;42(7):706–9. 10.1111/1346-8138.12861 [PubMed] [Cross Ref]
31. Grall A, Guaguère E, Planchais S, et al. : PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans. Nat Genet. 2012;44(2):140–7. 10.1038/ng.1056 [PubMed] [Cross Ref]
32. Baulande S, Langlois C.: [Proteins sharing PNPLA domain, a new family of enzymes regulating lipid metabolism]. Med Sci (Paris). 2010;26(2):177–84. 10.1051/medsci/2010262177 [PubMed] [Cross Ref]
33. Kienesberger PC, Oberer M, Lass A, et al. : Mammalian patatin domain containing proteins: a family with diverse lipolytic activities involved in multiple biological functions. J Lipid Res. 2009;50(Suppl):S63–8. 10.1194/jlr.R800082-JLR200 [PMC free article] [PubMed] [Cross Ref]
34. Fischer J, Lefèvre C, Morava E, et al. : The gene encoding adipose triglyceride lipase ( PNPLA2) is mutated in neutral lipid storage disease with myopathy. Nat Genet. 2007;39(1):28–30. 10.1038/ng1951 [PubMed] [Cross Ref]
35. Mubaidin A, Roberts E, Hampshire D, et al. : Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum. J Med Genet. 2003;40(7):543–6. 10.1136/jmg.40.7.543 [PMC free article] [PubMed] [Cross Ref]
36. Rainier S, Bui M, Mark E, et al. : Neuropathy target esterase gene mutations cause motor neuron disease. Am J Hum Genet. 2008;82(3):780–5. 10.1016/j.ajhg.2007.12.018 [PubMed] [Cross Ref]
37. Romeo S, Kozlitina J, Xing C, et al. : Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nat Genet. 2008;40(12):1461–5. 10.1038/ng.257 [PMC free article] [PubMed] [Cross Ref]
38. Boyden LM, Craiglow BG, Zhou J, et al. : Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia. J Invest Dermatol. 2015;135(6):1540–7. 10.1038/jid.2014.485 [PMC free article] [PubMed] [Cross Ref]
39. Laird DW.: Syndromic and non-syndromic disease-linked Cx43 mutations. FEBS Lett. 2014;588(8):1339–48. 10.1016/j.febslet.2013.12.022 [PubMed] [Cross Ref]
40. Martin PE, Easton JA, Hodgins MB, et al. : Connexins: sensors of epidermal integrity that are therapeutic targets. FEBS Lett. 2014;588(8):1304–14. 10.1016/j.febslet.2014.02.048 [PubMed] [Cross Ref]
41. Pfenniger A, Wohlwend A, Kwak BR.: Mutations in connexin genes and disease. Eur J Clin Invest. 2011;41(1):103–16. 10.1111/j.1365-2362.2010.02378.x [PubMed] [Cross Ref]
42. Macari F, Landau M, Cousin P, et al. : Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis. Am J Hum Genet. 2000;67(5):1296–301. 10.1016/S0002-9297(07)62957-7 [PubMed] [Cross Ref]
43. Richard G, Smith LE, Baily RA, et al. : Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nat Genet. 1998;20(4):366–9. 10.1038/3840 [PubMed] [Cross Ref]
44. Paznekas WA, Boyadjiev SA, Shapiro RE, et al. : Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia. Am J Hum Genet. 2003;72(2):408–18. 10.1086/346090 [PubMed] [Cross Ref]
45. Shao Q, Liu Q, Lorentz R, et al. : Structure and functional studies of N-terminal Cx43 mutants linked to oculodentodigital dysplasia. Mol Biol Cell. 2012;23(17):3312–21. 10.1091/mbc.E12-02-0128 [PMC free article] [PubMed] [Cross Ref]
46. Albert MR, Mackool BT.: Pityriasis rubra pilaris. Int J Dermatol. 1999;38(1):1–11. 10.1046/j.1365-4362.1999.00513.x [PubMed] [Cross Ref]
47. Braun-Falco O, Ryckmanns F, Schmoeckel C, et al. : Pityriasis rubra pilaris: a clinico-pathological and therapeutic study with special reference to histochemistry, autoradiography, and electron microscopy. Arch Dermatol Res. 1983;275(5):287–95. 10.1007/BF00417199 [PubMed] [Cross Ref]
48. Magro CM, Crowson AN.: The clinical and histomorphological features of pityriasis rubra pilaris. A comparative analysis with psoriasis. J Cutan Pathol. 1997;24(7):416–24. 10.1111/j.1600-0560.1997.tb00816.x [PubMed] [Cross Ref]
49. Soeprono FF.: Histologic criteria for the diagnosis of pityriasis rubra pilaris. Am J Dermatopathol. 1986;8(4):277–83. 10.1097/00000372-198608000-00001 [PubMed] [Cross Ref]
50. Auffret N, Quint L, Domart P, et al. : Pityriasis rubra pilaris in a patient with human immunodeficiency virus infection. J Am Acad Dermatol. 1992;27(2 Pt 1):260–1. 10.1016/S0190-9622(08)80734-7 [PubMed] [Cross Ref]
51. Klein A, Landthaler M, Karrer S.: Pityriasis rubra pilaris: a review of diagnosis and treatment. Am J Clin Dermatol. 2010;11(3):157–70. 10.2165/11530070-000000000-00000 [PubMed] [Cross Ref]
52. Menni S, Brancaleone W, Grimalt R.: Pityriasis rubra pilaris in a child seropositive for the human immunodeficiency virus. J Am Acad Dermatol. 1992;27(6 Pt 1):1009. 10.1016/S0190-9622(08)80267-8 [PubMed] [Cross Ref]
53. Griffiths WA.: Pityriasis rubra pilaris. Clin Exp Dermatol. 1980;5(1):105–12. 10.1111/j.1365-2230.1980.tb01676.x [PubMed] [Cross Ref]
54. Vasher M, Smithberger E, Lien MH, et al. : Familial pityriasis rubra pilaris: report of a family and therapeutic response to etanercept. J Drugs Dermatol. 2010;9(7):844–50. [PubMed]
55. Fuchs-Telem D, Sarig O, van Steensel MA, et al. : Familial pityriasis rubra pilaris is caused by mutations in CARD14. Am J Hum Genet. 2012;91(1):163–70. 10.1016/j.ajhg.2012.05.010 [PubMed] [Cross Ref]
56. Bertin J, Wang L, Guo Y, et al. : CARD11 and CARD14 are novel caspase recruitment domain (CARD)/membrane-associated guanylate kinase (MAGUK) family members that interact with BCL10 and activate NF-kappa B. J Biol Chem. 2001;276(15):11877–82. 10.1074/jbc.M010512200 [PubMed] [Cross Ref]
57. Scudiero I, Zotti T, Ferravante A, et al. : Alternative splicing of CARMA2/CARD14 transcripts generates protein variants with differential effect on NF-κB activation and endoplasmic reticulum stress-induced cell death. J Cell Physiol. 2011;226(12):3121–31. 10.1002/jcp.22667 [PMC free article] [PubMed] [Cross Ref]
58. Jordan CT, Cao L, Roberson ED, et al. : PSORS2 is due to mutations in CARD14. Am J Hum Genet. 2012;90(5):784–95. 10.1016/j.ajhg.2012.03.012 [PubMed] [Cross Ref]
59. Arita K, Jacyk WK, Wessagowit V, et al. : The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1. J Invest Dermatol. 2007;127(2):490–3. 10.1038/sj.jid.5700550 [PubMed] [Cross Ref]
60. Jacyk WK.: Bathing-suit ichthyosis. A peculiar phenotype of lamellar ichthyosis in South African blacks. Eur J Dermatol. 2005;15(6):433–6. [PubMed]
61. Oji V, Hautier JM, Ahvazi B, et al. : Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype. Hum Mol Genet. 2006;15(21):3083–97. 10.1093/hmg/ddl249 [PubMed] [Cross Ref]
62. Benmously-Mlika R, Zaouak A, Mrad R, et al. : Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child. Int J Dermatol. 2014;53(12):1478–80. 10.1111/ijd.12569 [PubMed] [Cross Ref]
63. Bourrat E, Blanchet-Bardon C, Derbois C, et al. : Specific TGM1 mutation profiles in bathing suit and self-improving collodion ichthyoses: phenotypic and genotypic data from 9 patients with dynamic phenotypes of autosomal recessive congenital ichthyosis. Arch Dermatol. 2012;148(10):1191–5. 10.1001/archdermatol.2012.1947 [PubMed] [Cross Ref]
64. Yamamoto M, Sakaguchi Y, Itoh M, et al. : Bathing suit ichthyosis with summer exacerbation: a temperature-sensitive case. Br J Dermatol. 2012;166(3):672–4. 10.1111/j.1365-2133.2011.10594.x [PubMed] [Cross Ref]
65. Boyden LM, Kam CY, Hernandez-Martin A, et al. : Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndrome. Hum Mol Genet. 2016;25(2):348–57. 10.1093/hmg/ddv481 [PMC free article] [PubMed] [Cross Ref]
66. Armstrong DK, McKenna KE, Purkis PE, et al. : Haploinsufficiency of desmoplakin causes a striate subtype of palmoplantar keratoderma. Hum Mol Genet. 1999;8(1):143–8. 10.1093/hmg/8.1.143 [PubMed] [Cross Ref]
67. Pigors M, Schwieger-Briel A, Cosgarea R, et al. : Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy. Acta Derm Venereol. 2015;95(3):337–40. 10.2340/00015555-1974 [PubMed] [Cross Ref]
68. Rampazzo A, Nava A, Malacrida S, et al. : Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy. Am J Hum Genet. 2002;71(5):1200–6. 10.1086/344208 [PubMed] [Cross Ref]
69. van der Zwaag PA, Jongbloed JD, van den BMP, et al. : A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy. Hum Mutat. 2009;30(9):1278–83. 10.1002/humu.21064 [PubMed] [Cross Ref]
70. Whittock NV, Ashton GH, Dopping-Hepenstal PJ, et al. : Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiency. J Invest Dermatol. 1999;113(6):940–6. 10.1046/j.1523-1747.1999.00783.x [PubMed] [Cross Ref]
71. Aldahmesh MA, Mohamed JY, Alkuraya HS, et al. : Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia. Am J Hum Genet. 2011;89(6):745–50. 10.1016/j.ajhg.2011.10.011 [PubMed] [Cross Ref]
72. Jakobsson A, Westerberg R, Jacobsson A.: Fatty acid elongases in mammals: their regulation and roles in metabolism. Prog Lipid Res. 2006;45(3):237–49. 10.1016/j.plipres.2006.01.004 [PubMed] [Cross Ref]
73. Leonard AE, Kelder B, Bobik EG, et al. : Identification and expression of mammalian long-chain PUFA elongation enzymes. Lipids. 2002;37(8):733–40. 10.1007/s11745-002-0955-6 [PubMed] [Cross Ref]
74. McMahon A, Butovich IA, Mata NL, et al. : Retinal pathology and skin barrier defect in mice carrying a Stargardt disease-3 mutation in elongase of very long chain fatty acids-4. Mol Vis. 2007;13:258–72. [PMC free article] [PubMed]
75. Poulos A, Beckman K, Johnson DW, et al. : Very long-chain fatty acids in peroxisomal disease. Adv Exp Med Biol. 1992;318:331–40. [PubMed]
76. Schneiter R, Brugger B, Amann CM, et al. : Identification and biophysical characterization of a very-long-chain-fatty-acid-substituted phosphatidylinositol in yeast subcellular membranes. Biochem J. 2004;381(Pt 3):941–9. 10.1042/BJ20040320 [PubMed] [Cross Ref]
77. Toulmay A, Schneiter R.: Lipid-dependent surface transport of the proton pumping ATPase: a model to study plasma membrane biogenesis in yeast. Biochimie. 2007;89(2):249–54. 10.1016/j.biochi.2006.07.020 [PubMed] [Cross Ref]
78. Vasireddy V, Uchida Y, Salem N, et al. : Loss of functional ELOVL4 depletes very long-chain fatty acids (or =C28) and the unique omega-O-acylceramides in skin leading to neonatal death. Hum Mol Genet. 2007;16(5):471–82. 10.1093/hmg/ddl480 [PMC free article] [PubMed] [Cross Ref]
79. Zhang K, Kniazeva M, Han M, et al. : A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy. Nat Genet. 2001;27(1):89–93. 10.1038/83817 [PubMed] [Cross Ref]

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