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

研究成果: Contribution to journalArticle査読

9 被引用数 (Scopus)

抄録

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.

本文言語英語
ページ(範囲)2187-2189
ページ数3
ジャーナルNeurology
53
9
DOI
出版ステータス出版済み - 12 10 1999

All Science Journal Classification (ASJC) codes

  • 臨床神経学

フィンガープリント

「Autosomal dominant familial spinal and bulbar muscular atrophy with gynecomastia」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル