口蓋裂の治療過程で発見したStickler症候群の4例

The Stickler syndrome (STL) is an autosomal dominant inherited disease caused by mutation of the collagen genes and is classified into STL1, STL2, and STL3. It is associated with eye manifestations, such as progressive myopia and retinal detachment, hypoplasia of the face, cleft palate, microgenia,...

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Bibliographic Details
Published in日本口腔外科学会雑誌 Vol. 58; no. 12; pp. 733 - 737
Main Authors 渡邊, 章, 内山, 健志, 村松, 恭太郎, 成田, 真人, 中野, 洋子, 高野, 伸夫
Format Journal Article
LanguageJapanese
Published 社団法人 日本口腔外科学会 20.12.2012
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