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  1. 学術雑誌論文
  2. 琉球医学会
  3. 琉球大学保健学医学雑誌
  4. 4巻3号
  1. 部局別インデックス
  2. その他

[原著]慢性肉芽腫症の1家系例

http://hdl.handle.net/20.500.12000/0002016393
http://hdl.handle.net/20.500.12000/0002016393
9ee39a81-ab79-45e0-96a5-753ba25add8e
名前 / ファイル ライセンス アクション
v4p247.pdf v4p247.pdf
Item type デフォルトアイテムタイプ(フル)(1)
公開日 2014-07-18
タイトル
タイトル [原著]慢性肉芽腫症の1家系例
言語 ja
作成者 大城, 隆

× 大城, 隆

ja 大城, 隆

平山, 清武

× 平山, 清武

ja 平山, 清武

屋良, 朝雄

× 屋良, 朝雄

ja 屋良, 朝雄

嘉陽, 宗俊

× 嘉陽, 宗俊

ja 嘉陽, 宗俊

臼井, 朋包

× 臼井, 朋包

ja 臼井, 朋包

Ohshiro, Takashi

× Ohshiro, Takashi

en Ohshiro, Takashi

Hirayama, Kiyotake

× Hirayama, Kiyotake

en Hirayama, Kiyotake

Yara, Asao

× Yara, Asao

en Yara, Asao

Kayo, Munetoshi

× Kayo, Munetoshi

en Kayo, Munetoshi

Usui, Tomofusa

× Usui, Tomofusa

en Usui, Tomofusa

アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
言語 ja
権利情報 琉球医学会
内容記述
内容記述タイプ Other
内容記述 Chronic granulomatous disease (CGD) is a hereditary disorder of phagocytes characterized by their defective microbicidal activity and is clinically manifested by recurrent and intractable bacterial infections. Since it was first reported in 1957, about sixty cases of this disease have been reported in the literature of Japan. Recently, we have encountered first case of CGD in Okinawa. The patient is an 11-months-old boy. He is the third of three siblings and his two sisters as well as his parents are in good health. Since newborn period, he has had recurrent purulent infection of the skin and cervical lymphnodes. He was first admitted to the our hospital at the age of 8 months with osteomyelitis and bronchopneumonia. Two months after discharge, he was re-admitted with Staphylococcal scalded skin syndrome(SSSS). Laboratory studies at the our hospital, including bone marrow cytology, levels of immunoglobulins, complements and lymphocyte subpopulation, were all within normal limits. The most remarkable laboratory finding in this patient was the failure to reduce NBT in leukocytes, suggesting that he had bactericidal abnormality. So, he was further evaluated for his immunologic state at the Hiroshima University School of Medicine, where he was made definitive diagnosis of an X-linked recessive type of CGD, and his mother was carrier.
内容記述タイプ Other
内容記述 論文
出版者
言語 ja
出版者 琉球大学医学部
言語
言語 jpn
資源タイプ
資源タイプ journal article
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0285-9270
収録物識別子タイプ NCID
収録物識別子 AN00250763
収録物名
言語 ja
収録物名 琉球大学保健学医学雑誌=Ryukyu University Journal of Health Sciences and Medicine
書誌情報
巻 4, 号 3, p. 247-254
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