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家族性贝克威思-维德曼综合征中父系印记的证据。

Evidence for paternal imprinting in familial Beckwith-Wiedemann syndrome.

作者信息

Viljoen D, Ramesar R

机构信息

Department of Human Genetics, University of Cape Town Medical School, South Africa.

出版信息

J Med Genet. 1992 Apr;29(4):221-5. doi: 10.1136/jmg.29.4.221.

Abstract

A previously unreported family in which seven members in two generations have Beckwith-Wiedemann syndrome (BWS) is documented. Paternal imprinting of the gene responsible for BWS is involved as the mechanism responsible for the aberrant inheritance pattern in this kindred. A review of published reports showed 27 previously published pedigrees with two or more affected subjects with BWS. Paternal imprinting would explain the non-mendelian inheritance of BWS in all but four kindreds. The latter families are examined in more detail and in only one example is the evidence against imprinting totally unexplained.

摘要

本文记录了一个此前未报道过的家族,该家族两代人中的七名成员患有贝克威思-维德曼综合征(BWS)。负责BWS的基因的父系印记参与其中,是该家族异常遗传模式的原因。对已发表报告的回顾显示,之前有27个家系发表过,其中有两名或更多受影响的BWS患者。父系印记可以解释除四个家系外所有BWS的非孟德尔遗传现象。对后四个家系进行了更详细的研究,只有一个家系中反对印记的证据完全无法解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b07/1015916/0fad8a3f2277/jmedgene00018-0008-a.jpg

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