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Angelman syndrome (AS) is a distinct neurogenetic syndrome, first described in 1965. The phenotype is well known in infancy and adulthood, but the clinical features may change with age. The main clinical characteristics include severe mental retardation, epileptic seizures and EEG abnormalilties, neurological problems and distinct facial dysmorphic features. Behavioural problems such as hyperactivity and sleeping problems are reported, although these patients present mostly a happy personality with periods of inappropriate laughter. Different underlying genetic mechanisms may cause AS, with deletion of chromosome 15 as the most frequent cause. Other genetic mechanisms such as paternal uniparental disomy, imprinting defect and mutation in the UBE3A gene are present in smaller groups of patients with AS. As the recurrence risk can be up to 50%, the clinical diagnosis of AS should be confirmed by laboratory tesing, and genetic counselling should be provided. Treatment of seizures, physical therapy or other intervention strategies are helpful to ameliorate the symptoms.
Angelman syndrome (AS) is a distinct neurogenetic syndrome, first described by Dr Harry Angelman in 1965, an English paediatrician, who described three severely mentally retarded children. AS presents with severe mental retardation, absent speech, periods of inappropriate laughter, microcephaly, macrostomia, maxillary hypoplasia, prognathia and neurological problems with a puppet-like gait, ataxia and epileptic seizures with specific EEG abnormalities.1 Patients have a happy and excitable personality. With advancing age, the typical phenotype becomes less striking because of the facial coarsening, thoracic scoliosis and mobility problems. Seizures remain present in adult AS patients, but hyperactivity, short attention span and sleeping problems improve in adulthood.2, 3, 4 The incidence of AS is estimated to be between 1/10000 and 1/20000.5 Different genetic mechanisms may cause AS, such as deletion of the 15q11.2-q13 critical region (60–75%), paternal uniparental disomy (UPD) (2–5%), mutations in the imprinting centre (2–5%) and mutation in the UBE3A gene (10%). In a group of 5–26% patients the diagnosis of AS is pure clinical and no genetic cause is found, although the recurrence risk can be as high as 50%.
In the newborn baby the phenotype seems to be normal. In the first 6 months of the neonatal period, feeding problems and muscle hypotonia may be present.5 At the age of 6 months there is a developmental delay. The diagnosis of AS is often difficult to suspect in infancy as developmental delay, hypotonia and other non-specific features usually emerge between 6 months and 2 years of age. However, the presence of tremulous movements or unsteady movements before walking may suggest the diagnosis of AS. From the age of 1 year, the typical features of AS become more clear such as severe mental retardation, absent speech, outbursts of laughter, microcephaly, macrostomia, maxillary hypoplasia, prognathia and neurological problems with a puppet-like gait, ataxia and epileptic seizures with specific EEG abnormalities. In childhood, a diversity of seizures was observed, such as tonic-clonic seizures, atypical absence seizures, myoclonic seizures, status epilepticus and absence status, and myoclonic status.6, 7 The most typical EEG finding in AS in children and adults is the presence of triphasic delta activity with a maximum over the frontal regions. The probability of having these triphasic waves increases with age and this EEG pattern can be helpful for making the diagnosis of AS in mentally retarded patients.1
The behavioural phenotype in these patients include a happy personality, there are outbursts of laughter often with hand flapping, hyperactivity without aggression, short attention span, excitability and sleeping problems with decreased need to sleep, increased sensitivity to heat, attraction to and fascination with water.1, 2, 3, 4, 8
Addendum 1 presents an overview of the recently updated diagnostic criteria (developmental, laboratory and clinical features) according to the Scientific Advisory Committee of the US Angelman Syndrome Foundation.1 Figure 1 presents several AS patients at different ages.
Life expectancy in AS seems to be nearly normal, but there are no data available. With advancing age the clinical picture may change and marked prognathism, macrostomia and prominent lower lip can be noted in adult AS patients, especially in those with increased mouthing behaviours and tongue protrusion and can be present both in patients with and without anti-epileptic drug treatment. About 90% of patients develop seizures at the first year of age. Although several authors2, 9, 10 reported a decrease of the epileptic seizures in adulthood, Laan et al7 observed that 92% of the adult patients still experienced epileptic seizures, with atypical absence seizures and myoclonic seizures being the most prominent.
Most AS patients have a stable vision without any type of degenerative retinopathy, although iris and choroidal hypopigmentation is to be expected in patients with a deletion of the 15q11.2-q13 critical region. Strabismus, optical nerve atrophy and blindness are rarely reported.11, 12
Thoracic scoliosis is reported in about 40% of the adults and mostly in females.13
With advancing age adults become less active and there is a tendency towards obesity. Mobility decreases with joint contractures leading to difficulties of walking and some patients become wheelchair bound.16
The use of special nipples may improve feeding in newborn AS babies with feeding difficulties. Gastroesophageal reflux is often present and requires upright positioning or specific motility medications. As the majority of the patients develop seizures at very young age early attention should be given to this possible complication, which needs anticonvulsant medications. As children may develop ocular problems, visual assessment is important to encourage interactions and diminish autistic and self-mutilative tendencies.17 Ocular surgery can be offered in patients with strabismus. A diet rich to fibers or laxative agents can be helpful in patients with constipation. Drooling in mentally retarded patients is often present but difficult to treat, and behavioural treatment should be considered.18 New surgical techniques on salivary duct reimplantation or ligation in this improving treatment area are valuable alternatives. In only one AS patient specific dental treatment was reported by Murakami et al.19 Orthopedic problems, such as subluxed or pronated ankles, tight Achilles tendons or scoliosis may be treated by bracing or even surgery. Vigilance of cardiac rhythm during anaesthesia and perioperative period is required.14, 15
Physical therapy is needed for the unstable or non-ambulatory children and for extremely atactic children adaptive chairs or positioners. With advancing age, adults become less active and the use of activity schedules may be helpful to prevent the extent of scoliosis and obesity. As decreased mobility leading to the difficulties of walking, prevention should be focused on the severe neurological instability by providing rehabilitative, early intervention and psychosocial services.17 Occupational therapy is needed to stimulate fine motor and oral-motor control skills. Speech therapy including nonverbal methods of communication, picture cards or communication boards should be introduced as active communication in this group of children is poorly developed.
Patients with excessive hypermotoric behaviour need a safe and adapted environment or may be treated with medication, but often patients benefit from both options. Sedative medication can be given in case of severe sleep problems. Melatonin may promote sleep in AS patients, but Braam et al20 observed that melatonin lost its beneficial effect after several weeks in most AS patients.
Owing to the presence of spastic paraplegia, the diagnosis of perinatal damage is often considered. In this group of mentally retarded patients, the typical EEG pattern can be helpful for the diagnosis of AS and differential diagnosis includes hypsarrhythmia in the West syndrome or the petit mal variant pattern in Lennox–Gastaut.
A portion of children with a clinical diagnosis of AS but without genetic confirmation, have mutations in the MECP2 gene confirming Rett syndrome.21 Certainly in the first few years of life Rett syndrome should be suspected in these AS-test negative girls.
Mowat–Wilson syndrome is caused by heterozygous deletions or truncating mutations in the ZFHX1B (SIP1) gene on 2q22. The facial features, severe mental retardation, microcephaly, seizures and short stature are resembling the AS.22
X-linked alpha-thalassemia/mental retardation syndrome (ATR-X) is caused by mutations in the XNP gene on Xq13. These patients have severe mental retardation, there is no speech development and seizures are common.23
The 22q13 deletion syndrome (Phelan–McDermid syndrome) with variable sizes of the deletion are often submicroscopic and requires special molecular cytogenetic methods to detect the deletion. Patients have global developmental delay, moderate to profound mental retardation, delay of speech development and mild dysmorphic features.24
Many microdeletions, with a wide spectrum of clinical features, can mimic the features of AS and the value of comparative genome hybridisation (CGH) is therefore a valuable tool in AS-test negative patients.
Different underlying genetic mechanisms may cause AS resulting in a comparable clinical phenotype with severe mental retardation, speech retardation and behavioural phenotype. However, differences in the clinical phenotype are observed in AS patients, with a different underlying genetic mechanism.25
A deletion or re-arrangement of the maternal chromosome 15 at locus 15q11-q13 is present in 60–75% of the patients. Patients with a deletion have a more severe clinical phenotype including microcephaly, motor difficulties, seizures and language impairment.1, 26, 27
A small percentage of patients (2–5%) have paternal UPD for chromosome 15.28 The UPD can be composed by both homologous chromosomes from one parent (heterodisomy) or by a duplication of one chromosome (isodisomy), or by a mixture of both these chromosomal compositions.29 Mechanisms of UPD formation are trisomy rescue, gamete complementation, mitotic duplication and post-fertilization errors.30 The mechanism of paternal UPD of chromosome 15 was described by Robinson et al,31 showing a somatic segregation error in about 75% of these paternal UPD15 cases. A milder clinical phenotype in patients with paternal UPD has been suggested compared with AS patients with a deletion.32, 33 This group of patients has less frequent microcephaly, motor and ataxia problems and seizures.1
Mutations in the imprinting centre (IC) (imprinting centre defect) are present in about 2–5% of the patients. Microcephaly, hypopigmentation, motor and ataxia problems and seizures are less frequent in this group of patients.1, 34 Some patients have more advanced speech abilities.35
The PWS/AS region contains a number of genes that are expressed exclusively from the paternal chromosome 15 (eg MKRN3, MAGEL2, NDN, SNURF-SNRPN, C15orf2 and PWRN1) or maternal chromosome 15 (eg UBE3A, ATP10A). Mutations in the UBE3A gene were first described in 1997 by Kishino et al36 and Matsuura et al37 and are present in about 10% of the patients. The cardinal features of AS are caused by deficient expression or function of the maternally inherited UBE3A allele in certain brain regions.13, 38, 39 Williams5 described the map of the 15q11.2-15q13 region showing the complex mechanism of controlling the transcription of the UBE3A gene by a distant imprinting control centre. The UBE3A gene shows biallellic expression in most tissues, but shows preferential expression of the maternal allele in the brain of humans and mice.40 The UBE3A gene produces the E6-associated protein (E6AP). This protein is acting as a cellular ligase enzyme to create a covalent linkage between the ubiquitin molecule and its target protein, which becomes polyubiquilated, and results finally in their degradation by the 26S proteasome, and plays thus a role in cellular protein homeostasis. Mutations in the UBE3A gene results in a disrupted functioning of the protein and could cause the mental retardation and seizures.5
In a group of 5–26% of the patients with the classical phenotypic AS features, the genetic defect remains unidentified.
The diagnosis of AS is a clinical diagnosis confirmed by laboratory testing (Figure 2).
A cytogenetically visible chromosome rearrangement involving the 15q11.2-q13 region on a standard chromosomal analysis such as large deletion, translocation or inversion is seen in <1% of the patients, but the 5–7Mb common deletion is not detected by routine chromosome analysis.
The DNA methylation test detects a deletion, UPD or an imprinting centre defect and confirms the diagnosis in about 78% of the patients. In addition, fluorescent in situ hybridisation studies (FISH) with the D15S10 and/or SNRPN probe detects a 4–6Mb deletion of the 15q11.2-q13 region in about 70% (60–75%) of the patients. An alternative method to detect a (smaller) deletion may be CGH.
Sequence analysis of the UBE3A gene detects mutations in about 10% of the patients.
In the remaining group of patients no further diagnostic approach is possible at this moment.
The recurrence risk of AS in subsequent children in families with a child with a de novo deletion is estimated ~1%.41 Kokkonen and Leisti42 reported two sibs who had an identical interstitial deletion in the maternal chromosome 5 suggesting the presence of germline mosaicism of del (15)(q11q13) in the mother.
In AS patients with a chromosomal rearrangement or small-inherited interstitial deletion the recurrence risk can be as high as 50%. Therefore, chromosomal and FISH analyses should be performed in the parents (mother) of an AS patient with a deletion, to rule out a chromosomal rearrangement in the parents and to determine whether the rearrangement is inherited or de novo in the AS patient.
Paternal UPD of chromosome 15 arises as a sporadic event with an extremely low, probably <1/200, recurrence risk. A chromosomal analysis, however, is indicated in an AS patient with a UPD, to rule out an inherited paternal 15;15 Robertsonian translocation, as the recurrence risk can be very high (almost 100%) in case the father is carrier of a 15;15 Robertsonian translocation.
The risk to subsequent children in case of an AS patient with an IC defect can be as high as 50%. A patient with a deletion in the IC can have a phenotypically normal mother who also has an IC deletion, inherited from her father or acquired by a spontaneous mutation on her paternal chromosome 15, and in this situation the recurrence risk is 50%.43 The recurrence risk in patients with an imprinting centre defect without a deletion, probably as the result of a de novo defect of the imprinting process during the oogenesis of the mother, is estimated <1%, and this is the case in 80% of patients with an IC defect.44
In 10% of the AS patients, a UBE3A gene mutation is present and can be de novo or inherited.37, 39 Females carrying a UBE3A gene mutation, without having AS because the gene is silenced, have a recurrence risk of 50% for a child with AS in each pregnancy. In case of a de novo UBE3A gene mutation in the proband, the recurrence risk is nearly 0%. However, germline mosaicism was described in several families with affected siblings but without a mutation in the mother.45
In the remaining group of patients without a proven genetic defect the recurrence risk remains undetermined but may be high (up to 50%) (see also Figure 2).
Developmental history and laboratory findings:
Clinical features of AS1
A. Consistent features (100%)
B. Frequent features (more than 80%)
C. Associated features (20–80%)