[Current diagnosis in muscular dystrophies. New developments, methods of examination and case examples]

Nervenarzt. 1999 Feb;70(2):89-100. doi: 10.1007/s001150050408.
[Article in German]

Abstract

Recent progress in the field of molecular genetics revealed a broader spectrum of dystrophin-related disorders than previously assumed. In addition, the pathogenetic basis of other types of muscular dystrophies could be identified: some autosomal-recessive limb girdle dystrophies are caused by mutations of sarcoglycan genes, others are caused by deficiency of the sarcoplasmatic enzyme calpain-3. Emery-Dreifuss muscular dystrophy is due to the deficiency of the nuclear membrane protein emerin. About 50% of congenital muscular dystrophies are related to mutations of a extracellular matrix protein merosin (alpha-laminin). A series of monoclonal antibodies for immunohistochemistry is now available recognizing many cytoskeletal muscle proteins. In combination with molecular genetics a diagnostic flow chart can be developed which allows a definite diagnosis in most cases. In this review disease entities are illustrated by case reports. We discuss the significance of immunohistochemical and molecular methods for diagnosis.

Publication types

  • Case Reports
  • English Abstract
  • Review

MeSH terms

  • Adult
  • Biopsy
  • Child
  • Child, Preschool
  • DNA Mutational Analysis
  • Diagnosis, Differential
  • Dystrophin / genetics
  • Humans
  • Male
  • Muscle, Skeletal / pathology
  • Muscular Dystrophies / classification
  • Muscular Dystrophies / diagnosis*
  • Muscular Dystrophies / genetics

Substances

  • Dystrophin