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Scalp–ear–nipple syndrome (also known as "Finlay–Marks syndrome") is a condition associated with aplasia cutis congenita. ==Clinical features== The key affected features of this condition are described in its name. Scalp: There are raised nodules over the posterior aspect of the scalp, covered by scarred non-hair bearing skin. Ears: The shape of the pinnae is abnormal, with the superior edge of the pinna being turned over more than usual. The size of the tragus, antitragus and lobule may be small. Nipples: The nipples are absent or rudimentary. The breasts may be small or virtually absent. Other features of the condition〔Sobreira NL, Brunoni D, Cernach MC, Perez AB. Finlay-Marks (SEN) syndrome: a sporadic case and the delineation of the syndrome. Am J Med Genet A. 2006 Feb 1;140(3):300-2.〕 include: Dental abnormalities: missing or widely spaced teeth Syndactyly: toes or fingers may be partially joined proximally 〔〔〔〔 Erratum in: Am J Med Genet A. 2005 Jul 1;136(1):114-5.〕 Renal abnormalities: renal hypoplasia, pyeloureteral duplication Eye abnormalities: Cataract,〔 coloboma of the iris and asymmetric pupils.〔 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「Scalp–ear–nipple syndrome」の詳細全文を読む スポンサード リンク
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