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Median cleft of the upper lip associated with lipomas of the central nervous system and cutaneous polyps.

作者信息

Pai G S, Levkoff A H, Leithiser R E

出版信息

Am J Med Genet. 1987 Apr;26(4):921-4. doi: 10.1002/ajmg.1320260421.

DOI:10.1002/ajmg.1320260421
PMID:3591835
Abstract

An unusual combination of three rare developmental anomalies, ie, complete median cleft lip, cutaneous polyps, and midline lipomas of the central nervous system, was discovered in a male newborn. Inguinal hernia, cryptorchidism, and clinodactyly of the fifth fingers were other features. His mother was found to have clinodactyly, antimongoloid slant to her palpebral fissures, and computed tomography (CT) scan evidence of asymptomatic hydrocephaly. Family history and clinical investigations did not reveal any clues to etiology. This combination of findings may represent a new syndrome or another expression of frontonasal dysplasia.

摘要

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