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Apparent Malpuech syndrome: report on three Brazilian patients with additional signs.

作者信息

Guion-Almeida M L

机构信息

Servico de Genética Clínica, Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Bauru, Brazil.

出版信息

Am J Med Genet. 1995 Jul 31;58(1):13-7. doi: 10.1002/ajmg.1320580104.

Abstract

We report on 3 unrelated Brazilian patients with shortness of stature, hypertelorism, eye anomalies, facial clefting, hearing loss, urogenital abnormalities, omphalocele, "caudal appendage," and mental retardation. Two patients were born to normal and non-consanguineous parents and one was born to consanguineous (first cousin) parents (F = 1/16). The similarity of our patients with those previously reported by Malpuech et al. [Am J Med Genet 16:475-480, 1983] led us to suggest that they have the same condition.

摘要

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