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Schöpf–Schulz–Passarge syndrome : ウィキペディア英語版 | Schöpf–Schulz–Passarge syndrome
Schöpf–Schulz–Passarge syndrome (also known as "Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis") is an autosomal recessive condition with diffuse symmetric palmoplantar keratoderma, with the palmoplantar keratoderma and fragility of the nails beginning around age 12.〔Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.〕 It was characterized in 1971. It has been associated with WNT10A. == See also ==
* Palmoplantar keratoderma * List of cutaneous conditions * List of dental abnormalities associated with cutaneous conditions * List of cutaneous neoplasms associated with systemic syndromes
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「Schöpf–Schulz–Passarge syndrome」の詳細全文を読む
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