Marked hemiatrophy in carriers of Duchenne muscular dystrophy

Arch Neurol. 2010 Apr;67(4):497-500. doi: 10.1001/archneurol.2010.58.

Abstract

Objective: To describe the clinical and molecular genetic findings in 2 carriers of Duchenne muscular dystrophy (DMD) who exhibited marked hemiatrophy. Duchenne muscular dystrophy is an X-linked disorder in which affected male patients harbor mutations in the dystrophin gene. Female patients with heterozygous mutations may be manifesting carriers.

Design: Case study.

Setting: Neurology clinic.

Patients: Two manifesting carriers of DMD.

Interventions: Clinical and radiologic examinations along with histologic and molecular investigations.

Results: Both patients had marked right-sided hemiatrophy on examination with radiologic evidence of muscle atrophy and fatty replacement on the affected side. In each case, histologic analysis revealed a reduction in dystrophin staining on the right side. Genetic analysis of the dystrophin gene revealed a tandem exonic duplication in patient 1 and a multiexonic deletion in patient 2 with no further point mutations identified on the other chromosome.

Conclusions: Marked hemiatrophy can occur in DMD manifesting carriers. This is likely to result from a combination of skewed X-inactivation and somatic mosaicism.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Arm / pathology
  • Arm / physiopathology
  • DNA Mutational Analysis
  • Dystrophin / genetics
  • Exons / genetics
  • Female
  • Functional Laterality / physiology
  • Genetic Diseases, X-Linked / genetics
  • Genetic Diseases, X-Linked / pathology
  • Genetic Diseases, X-Linked / physiopathology
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Genotype
  • Heterozygote*
  • Humans
  • Leg / pathology
  • Leg / physiopathology
  • Magnetic Resonance Imaging
  • Middle Aged
  • Mosaicism
  • Muscle, Skeletal / pathology*
  • Muscle, Skeletal / physiopathology
  • Muscular Atrophy / genetics*
  • Muscular Atrophy / pathology*
  • Muscular Atrophy / physiopathology
  • Muscular Dystrophy, Duchenne / genetics*
  • Mutation / genetics
  • X Chromosome Inactivation / genetics

Substances

  • Dystrophin