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The DNA diagnosis for bulbospinal muscular atrophy.

Abstract
We showed the analysis of the androgen receptor gene in 6 patients with bulbospinal muscular atrophy (BSMA). Four of them had typical manifestations of Kennedy's disease, while the other 2 patients did not show androgen insensitive signs such as gynecomastia or testicular atrophy. Enlarged CAG repeats were found in 4 patients with typical Kennedy's disease and 1 patient without androgen insensitive signs. This fact suggests that the DNA diagnosis by analysis of the androgen receptor gene is very useful to distinguish Kennedy's disease from other forms of BSMA.
AuthorsM Ohno, T Yamada, T Kobayashi, I Goto
JournalClinical neurology and neurosurgery (Clin Neurol Neurosurg) Vol. 96 Issue 1 Pg. 20-3 (Feb 1994) ISSN: 0303-8467 [Print] Netherlands
PMID8187377 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Receptors, Androgen
  • DNA
Topics
  • DNA (genetics)
  • Electrophoresis, Agar Gel
  • Genes, Recessive (genetics)
  • Humans
  • Male
  • Middle Aged
  • Muscular Atrophy, Spinal (diagnosis, genetics)
  • Neurologic Examination
  • Phenotype
  • Polymerase Chain Reaction (methods)
  • Receptors, Androgen (genetics)
  • Sex Chromosome Aberrations (diagnosis, genetics)
  • X Chromosome

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