A new phenotype of dysferlinopathy with congenital onset

C. Paradas, L. González-Quereda, N. De Luna, E. Gallardo, I. García-Consuegra, H. Gómez, A. Cabello, I. Illa, P. Gallano

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50 Citations (Scopus)


We report two patients with a new phenotype of dysferlinopathy presenting as congenital muscular disease. Both patients showed weakness in proximal lower limbs and neck flexor muscles at birth. The presence of normal CK levels during the first years should be noted. Initial MRI showed no abnormalities but short-time-inversion-recovery (STIR) sequences revealed a striking myoedema in gastrocnemius and hamstring muscles at the age of 5. Muscle biopsy showed mild dystrophic features and the absence of dysferlin. Dysferlin gene (DYSF) analysis revealed a p.Ala927LeufsX21 mutation in a homozygous state in both siblings. This new phenotype widens the clinical spectrum of dysferlin myopathies. © 2008 Elsevier B.V. All rights reserved.
Original languageEnglish
Pages (from-to)21-25
JournalNeuromuscular Disorders
Issue number1
Publication statusPublished - 1 Jan 2009


  • Congenital muscular dystrophy
  • Dysferlin
  • LGMD2B


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