Schwartz-Jampel syndrome (chondrodystrophic myotonia)

J Med Genet. 1992 Jan;29(1):58-62. doi: 10.1136/jmg.29.1.58.

Abstract

Schwartz-Jampel syndrome is a rare autosomal recessive disorder. Joint contractures, generalised myotonia, skeletal anomalies, and facial dysmorphism are common features; malignant hyperthermia is a potentially lethal complication during anaesthesia.

Publication types

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

MeSH terms

  • Adult
  • Child
  • Genes, Recessive
  • Humans
  • Male
  • Osteochondrodysplasias / diagnosis
  • Osteochondrodysplasias / genetics*