@article{oai:niigata-u.repo.nii.ac.jp:00021287,
 author = {田中, 正美},
 issue = {8},
 journal = {新潟医学会雑誌, 新潟医学会雑誌},
 month = {Aug},
 note = {Two siblings with decreased subcutaneous adipose tissue, muscular atrophy, joint contractures, recurrent skin eruptions and hyper-γ-globulinemia are reported. Patients showed reduced natural killer cell activity. The skin eruptions disappeared with prednisolone therapy. The clinical symptoms of these patients share some features with partial lipodystrophy but our patients are considered to be distinct from partial lipodystrophy since muscular atrophy, joint contractures and recurrent skin eruptions haye not been found in patients with partial lipodystrophy. Other Japanese nineteen patients with similar clinical manifestations have been reported. We propose that these patients show a distinct clinical entity.},
 pages = {503--508},
 title = {関節拘縮, 結節性紅斑, 高γ-グロブリン血症を伴う常染色体劣性遺伝形式を示す脂肪筋萎縮症 : 新しい症候群の提唱},
 volume = {105},
 year = {1991}
}