A novel syndrome of episodic muscle weakness maps to xp22.3

Am J Hum Genet. 1999 Oct;65(4):1104-13. doi: 10.1086/302588.

Abstract

We describe a family with a novel disorder characterized by episodic muscle weakness and X-linked inheritance. Eight males in three generations demonstrate the characteristic features of the disorder. Episodes of severe muscle weakness are typically precipitated by febrile illness and affect the facial and extraocular musculature, as well as the trunk and limbs, and resolve spontaneously over a period of weeks to months. Younger members of the family are normal between episodes but during relapses show generalized weakness, ptosis, and fluctuations in strength. In some cases, fatigability can be demonstrated. The proband has late-onset chronic weakness and fatigability. The clinical phenotype has features suggestive both of the congenital myasthenic syndromes and of ion-channel disorders such as the periodic paralyses. We have localized the responsible gene to chromosome Xp22.3, with a maximum two-point LOD score of 4. 52 at a recombination fraction of.0, between OACA2 and DXS9985.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age of Onset
  • Aged
  • Child
  • Child, Preschool
  • Chronic Disease
  • Crossing Over, Genetic / genetics
  • Female
  • Genetic Linkage / genetics*
  • Humans
  • Infant
  • Lod Score
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Muscle Weakness / epidemiology
  • Muscle Weakness / genetics*
  • Muscle Weakness / pathology
  • Muscle Weakness / physiopathology*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Muscle, Skeletal / physiopathology
  • Myasthenic Syndromes, Congenital / physiopathology
  • Paralyses, Familial Periodic / physiopathology
  • Pedigree
  • Phenotype
  • Polymorphism, Genetic / genetics
  • Syndrome
  • X Chromosome / genetics*

Associated data

  • OMIM/300000
  • OMIM/300500
  • OMIM/301200
  • OMIM/309801
  • OMIM/311860