Autosomal dominant familial spinal and bulbar muscular atrophy with gynecomastia

K. Ikezoe, T. Yoshimura, T. Taniwaki, E. Matsuura, H. Furuya, T. Yamada, K. Nagamatsu, Jun ichi Kira

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

The proband, a 53-year-old man, developed progressive spinal and bulbar muscular atrophy and gynecomastia at the age of 50. His father had weakness of lower limbs, and his son had a nasal voice, ocular movement abnormalities, and gynecomastia, whereas two of the proband's brothers showed either gynecomastia or tongue fasciculations. None of the patients showed any expansion of CAG repeat in the androgen receptor gene or any hormonal abnormality. Thus, this family is affected by a form of autosomal dominant spinal and bulbar muscular atrophy with gynecomastia.

Original languageEnglish
Pages (from-to)2187-2189
Number of pages3
JournalNeurology
Volume53
Issue number9
Publication statusPublished - Dec 10 1999

All Science Journal Classification (ASJC) codes

  • Clinical Neurology

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