Clinical and electrophysiological features in Chinese patients with Kennedy's disease

Clin Neurol Neurosurg. 2004 Sep;106(4):309-12. doi: 10.1016/j.clineuro.2004.02.002.

Abstract

Kennedy's disease is a X-linked neuromuscular disorder caused by an expanded trinucleotide repeat in the androgen receptor gene. To ascertain the clinical diagnosis of Kennedy's disease in a Chinese population, we used a rapid, accurate PCR-based sizing method for the CAG repeat allelotype. The clinical and electrophysiological features of affected patients are described. The CAG repeats ranged from 43 to 53 and were inversely correlated with the age of onset (r = -0.63; P < 0.005).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Adult
  • Asian Continental Ancestry Group* / genetics
  • Blood Glucose / metabolism
  • Creatine Kinase / blood
  • Female
  • Humans
  • Male
  • Middle Aged
  • Muscular Atrophy, Spinal / blood
  • Muscular Atrophy, Spinal / ethnology*
  • Muscular Atrophy, Spinal / physiopathology*
  • Neural Conduction / physiology
  • Receptors, Androgen / genetics
  • Trinucleotide Repeat Expansion

Substances

  • AR protein, human
  • Blood Glucose
  • Receptors, Androgen
  • Creatine Kinase