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两例同胞患无氨甲蝶呤的氨甲蝶呤综合征(ASSA):该综合征的进一步描述及文献综述

Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.

作者信息

Krajewska-Walasek M

机构信息

Department of Genetics, Memorial Hospital-Child Health Centre, Warsaw, Poland.

出版信息

Genet Couns. 1994;5(4):345-55.

PMID:7888136
Abstract

In this report we describe two sibs with an unusual and complex pattern of severe malformations resembling Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome, the phenotypic features of which are similar to those of aminopterin embryopathy. Six nonfamilial cases of ASSAS have been published in the literature to date. Our family with two affected sibs of different sexes supports the previous suggestion of autosomal recessive inheritance. Consanguinity of parents was excluded in this family, just as in all of the previously reported cases. Similar cases from the literature are briefly reviewed.

摘要

在本报告中,我们描述了两名患有异常且复杂的严重畸形模式的同胞,其类似于无氨甲蝶呤的氨甲蝶呤综合征(ASSA)综合征,该综合征的表型特征与氨甲蝶呤胚胎病相似。迄今为止,文献中已发表了6例非家族性ASSA病例。我们这个有两名不同性别的患病同胞的家族支持先前关于常染色体隐性遗传的推测。与所有先前报道的病例一样,该家族排除了父母近亲结婚的情况。文中简要回顾了文献中类似的病例。

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