Japanese
English
Neurological CPC・44
両下肢近位筋優位の筋萎縮を呈した22歳男性
A 22-year-old Man with Long-standing Weakness and Atrophy Predominantly in the Lower Extremities
森 秀生
1
,
佐藤 健一
1
,
平澤 恵理
1
,
近藤 智善
1
,
水野 美邦
1
Hideo Mori
1
,
Ken-ichi Sato
1
,
Eri Hirasawa
1
,
Tomoyoshi Kondo
1
,
Yoshikuni Mizuno
1
1順天堂大学医学部脳神経内科
1Department of Neurology, Juntendo University School of Medicine
キーワード：
congenital myopathy
,
congenital fiber type disproportion
,
nemaline myopa-thy
,
glycogen storage disease
,
debrancher deficiency
Keyword:
congenital myopathy
,
congenital fiber type disproportion
,
nemaline myopa-thy
,
glycogen storage disease
,
debrancher deficiency
pp.763-771
発行日 1996年8月1日
Published Date 1996/8/1
DOI https://doi.org/10.11477/mf.1406900991
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症例呈示
症例 Y．T．，22歳，男性。
主訴 両下肢近位筋優位の筋力低下，筋萎縮。
既往歴 12歳時左中耳炎。
We report a right-handed 22-year-old man with muscle atrophy. His prenatal course and the deliv-ery were uneventful, but he walked unsupported at 15 months of the age for the first time. He was apparently well but he was in the slowest group in running in schools. He noted a difficulty in climbing up stairs at 19 years of the age, and he was admitted to our hospital for the work up when he was 22-year-old. His family history and past medical history were unremarkable.
On admission, he was a slender and tall guy in no acute distress.
Copyright © 1996, Igaku-Shoin Ltd. All rights reserved.
