Hereditary Lipo-Muscular Atrophy with Joint Contracture, Skin Eruptions and Hyper-.GAMMA.-Globulinemia: a New Syndrome.

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概要

• 論文の詳細を見る

• We previously reported two siblings with decreased subcutaneous adipose tissue, muscular atrophy, joint contractures, recurrent skin eruptions, hyper-γ-globulinemia, and reduced natural killer cell activity. Some of their clinical features are similar to those of partial lipodystrophy, but they are distinct in that muscular atrophy, joint contractures and recurrent skin eruptions are not found in patients with partial lipodystrophy. Thirteen other Japanese patients with similar clinical manifestations have been reported. We propose that such cases should be considered a distinct clinical entity.(Internal Medicine 32: 42-45, 1993)

• 社団法人　日本内科学会の論文

著者

• YAMADA Shigeru

  the Department of Social Systems Engineering, the Faculty of Engineering, Tottori University

• Yuasa Tatsuhiko

  The Department Of Neurology School Of Medicine Tokyo Medical And Dental University

• Tanaka Masami

  The Department Of Internal Medicine Misato Kenwa Hospital

• Tanaka Keiko

  The Department Of Dermatology Tottori University School Of Medicine

• TSUBAKI Tadao

  the Department of Neurology, Tokyo Metropolitan Neurological Hospital

• TOYOSHIMA Itaru

  the Department of Neurology, Brain Research Institute, Niigata University

• MIYATAKE Tadashi

  the Department of Neurology, Brain Research Institute, Niigata University

• MIYATANI Nobuyuki

  the Department of Neurology, Brain Research Institute, Niigata University

• MIYASHITA Kotaro

  the Department of Neurology, Brain Research Institute, Niigata University

• SAKUMA Kaori

  the Department of Neurology, Brain Research Institute, Niigata University

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• Hereditary Lipo-Muscular Atrophy with Joint Contracture, Skin Eruptions and Hyper-.GAMMA.-Globulinemia: a New Syndrome.

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