@article{oai:u-ryukyu.repo.nii.ac.jp:02016424,
 author = {高木, 繁幸 and 比嘉, 秀正 and 空閑, 茂樹 and Takaki, Shigeyuki and Higa, Hidemasa and Kuga, Shigeki},
 issue = {3},
 journal = {琉球大学保健学医学雑誌＝Ryukyu University Journal of Health Sciences and Medicine},
 note = {A case of familial Wilson's disease was reported. A 14-year-old schoolboy complaining slow, low voice and dystonia and tremor of the Lt. upper extremity was found to have wilson's disease. One of his three brethren was found to have a asymptomatic addominal Wilson's disease. His neurological examination revealed, Kayser-Fleischer ring, saccadic eye movements, slow movement of the tongue, vacuous smile, systonia, rigidity in the all extremities, especially severe in the Lt. upper extremity. Tremor was found in the Lt. upper extremity. Deep tendon reflexes were generally exaggerated. The serum ceruloplasmin and serum copper were reduced m the patient and his young sister. D-penicillamine treatment in this patient triggered a febrile penicillamine eruption severe enough as if to suspect a measles. Desensitization was accomplished by starting at low doses of penicillamine and increasing at weekly intervals. The combined corticosterolds therapy was necessary., 論文},
 pages = {268--273},
 title = {[原著]Febrile penicillamine eruptionを発症した Wilson 病の同胞例},
 volume = {2}
}