Viljoen D, Ramesar R
Department of Human Genetics, University of Cape Town Medical School, South Africa.
J Med Genet. 1992 Apr;29(4):221-5. doi: 10.1136/jmg.29.4.221.
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.
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。