Search tips
Search criteria 


Logo of ngLink to Publisher's site
Neurol Genet. 2017 August; 3(4): e167.
Published online 2017 July 10. doi:  10.1212/NXG.0000000000000167
PMCID: PMC5524525

Novel fukutin mutations in limb-girdle muscular dystrophy type 2M with childhood onset

Limb-girdle muscular dystrophies (LGMDs) are a heterogeneous group of childhood- or adult-onset inherited neuromuscular disorders, which are characterized by weakness and wasting of proximal limb and axial muscles. LGMDs are divided into 8 autosomal-dominant (LGMD1)1 and 25 autosomal-recessive (LGMD2) forms ( One autosomal-recessive form is the LGMD2M (new nomenclature: Muscular Dystrophy-Dystroglycanopathy, type C, 4, MDDGC4, MIM #611588), which is caused by homozygous or compound heterozygous mutations in the fukutin gene (FKTN; MIM #607440) on chromosome 9q31.2. The LGMD2M, as the clinical mild end of fukutin-related muscle dystrophy without mental retardation, is rare worldwide and described mostly in individuals of non-Japanese descent (table e-1 at,5

Here, we report the second German case with an LGMD2M phenotype and describe 2 previously unreported mutations in the FKTN gene in a German female patient.

Clinical case presentation.

A 32-year-old female patient was admitted to our Neuromuscular Center. Written consent was obtained for the use of all clinical and diagnostic data. The patient was born to healthy nonconsanguineous parents. At the age of 7 years, cramping muscle pain, especially in the thighs, started and was accompanied by creatine kinase (CK) elevation. A muscle biopsy record described a chronic myopathic pattern and marked inflammation. The patient was treated with a corticosteroid, which profoundly reduced the CK level. In the following years, the patient developed a slowly progressive muscle weakness of both legs. At the age of 16 years, problems in climbing stairs and lifting heavy objects were noted. At the time of admission, the patient started to use a wheelchair for outdoor activities.

Neurologic examination revealed normal intellectual status, cranial nerve function, and sensorium. Inspection showed scapular winging, calf muscle enlargement, toe walking, and lumbar hyperlordosis (figure, A and D). We observed muscular atrophy with accentuation of the proximal lower extremities and reduced muscle strength. Gower and Trendelenburg signs were positive. Deep tendon reflexes were diminished. The patient also suffered from mild dysphagia and respiratory distress. EMG showed myopathic changes. Muscular MRI revealed a pronounced lipodystrophy of proximal upper and lower limb and limb-girdle muscles (figure, B, C, E, G, and H).

Clinical presentation and imaging findings in the patient

A multigene panel for LGMDs by next-generation sequencing (NGS) on genomic DNA isolated from a blood sample of our patient was performed. Coding and flanking sequences of all relevant genes were enriched using Agilent SureSelect technology. Massively parallel sequencing was performed using the HiSeq 2500 Sequencing platform from Illumina. Sanger sequencing was used for badly covered regions and validation of potentially pathogenic mutations.

In our patient, 2 novel missense mutations c.895A>C; p.Ser299Arg and c.1325A>G; p.Asn442Ser of the FKTN gene (NM_001079802.1) were found by NGS analysis and confirmed by Sanger sequencing. Both mutations disturb highly conserved positions in the fukutin protein. Several in silico prediction programs (MutationTaster, PolyPhen-2, SIFT) indicated that these mutations are most likely damaging. In Exome Aggregation Consortium (ExAC) and in Exome Server Browser, the variant c.895A>C was detected in heterozygous state only in one person, whereas the variant c.1325A>G had not been observed before.

With only one mutation c.1325A>G present in the father, a compound heterozygosity of the 2 mutations in our patient is strongly implied. Based on all information, we predict these 2 mutations as causative for the patients' disease.


Mutations in FKTN cause a wide clinical spectrum of myopathies: from severe congenital forms of muscular dystrophy with additional extramuscular symptoms to a milder form of LGMD2M, which is normally not associated with cognitive impairment.2 In the phenotypical spectrum of FKTN mutations, the classification from congenital muscular dystrophy (CMD) to LGMD2M was defined according to the onset of weakness.2 In practice, patients might display a phenotype well in between CMD and LGMD,2,6 pointing to an inherent difficulty of a strict classification. The phenotype of our patient is characterized by childhood onset, hypertrophy of calves, normal intelligence, and initial responsiveness to steroids.

The reduced ability of our patient to walk in her teens is in line with previous reports.7 In addition, we can provide clinical data of our patient until the age of 32 years. Our patient initially responded to steroid therapy, which might be explained by the profound inflammation in the muscle biopsy, comparable with the positive effect of steroids in Duchenne muscular dystrophy.

We show a rare case of LGMD2M and provide further insight into heterogeneity of phenotypes caused by mutations in FKTN and underline the importance of broad genetic assessment to provide correct diagnosis and to facilitate individual treatment in the future.

Supplementary Material

Data Supplement:


Supplemental data at

Author contributions: Mateja Smogavec and Jana Zschüntzsch: case report study and concept and design. Wolfram Kress: analysis and interpretation of data and critical revision of manuscript. Julia Mohr: analysis and interpretation of data. Peter Hellen: interpretation of radiologic imaging. Barbara Zoll: critical revision of the manuscript. Silke Pauli and Jens Schmidt: case report study concept and critical revision of the manuscript.

Study funding: No targeted funding reported.

Disclosure: M. Smogavec reports no disclosures. J. Zschüntzsch has received travel funding/speaker honoraria from Biotest AG and Grifols. W. Kress reports no disclosures. J. Mohr has been an employee of CeGaT GmbH and Praxis für Humangenetik. P. Hellen, B. Zoll, and S. Pauli report no disclosures. J. Schmidt has served on scientific advisory boards for BioMarin and CSL Behring; has received travel funding/speaker honoraria from Bayer, Biogen, Biotest, CSL Behring, Grifols, Novartis, Octapharma, and VitalAire; has served on the editorial boards of BMC Neurology, American Journal of Neuroscience, Edorium Journal of Neurology, World Journal of Neurology, and Journal of Neuromuscular Diseases; has been a consultant for Novartis and CSL Behring; and has received research support from Biogen, CSL Behring, Novartis, Octapharma, Association francaise contre les myopathies, and Deutsche Gesellschaft für Muskelkranke. Go to for full disclosure forms. The Article Processing Charge was funded by Institute of Human Genetics Goettingen.


1. Nigro V, Savarese M Genetic basis of limb-girdle muscular dystrophies: the 2014 update. Acta Myol 2014;33:1–12. [PMC free article] [PubMed]
2. Godfrey C, Clement E, Mein R, et al. Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. Brain 2007;130:2725–2735. [PubMed]
3. Vuillaumier-Barrot S, Quijano-Roy S, Bouchet-Seraphin C, et al. Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype. Neuromuscul Disord 2009;19:182–188. [PubMed]
4. Saredi S, Ruggieri A, Mottarelli E, et al. Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement. Muscle Nerve 2009;39:845–848. [PubMed]
5. Puckett RL, Moore SA, Winder TL, et al. Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardation. Neuromuscul Disord 2009;19:352–356. [PMC free article] [PubMed]
6. Ceyhan-Birsoy O, Talim B, Swanson LC, et al. Whole exome sequencing reveals DYSF, FKTN, and ISPD mutations in congenital muscular dystrophy without brain or eye involvement. J Neuromuscul Dis 2015;2:87–92. [PMC free article] [PubMed]
7. Riisager M, Duno M, Hansen FJ, Krag TO, Vissing CR, Vissing J A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy. Neuromuscul Disord 2013;23:562–567. [PubMed]

Articles from Neurology: Genetics are provided here courtesy of American Academy of Neurology