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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Published in | 日本口腔外科学会雑誌 Vol. 58; no. 12; pp. 733 - 737 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
社団法人 日本口腔外科学会
20.12.2012
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Subjects | |
Online Access | Get full text |
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