Suppr超能文献

家族性普拉德-威利综合征:病例报告及文献综述。

Familial Prader-Willi syndrome: case report and a literature review.

作者信息

McEntagart M E, Webb T, Hardy C, King M D

机构信息

The Children's Hospital, Dublin 1, Ireland, UK.

出版信息

Clin Genet. 2000 Sep;58(3):216-23. doi: 10.1034/j.1399-0004.2000.580309.x.

Abstract

Prader-Willi syndrome (PWS) is a neurobehavioural disorder arising through a number of different genetic mechanisms. All involve loss of paternal gene expression from chromosome 15q11q13. Although the majority of cases of PWS are sporadic, precise elucidation of the causative genetic mechanism is essential for accurate genetic counselling as the recurrence risk varies according to the mechanism involved. A pair of siblings affected by PWS is described. Neither demonstrates a microscopically visible deletion in 15q11q13 or maternal disomy. Methylation studies at D15S63 and at the SNRPN locus confirm the diagnosis of PWS. Molecular studies reveal biparental inheritance in both siblings with the exception of D15S128 and D15S63 where no paternal contribution is present indicating a deletion of the imprinting centre. Family studies indicate that the father of the siblings carries the deletion which, he has inherited from his mother. The recurrence risk for PWS in his offspring is 50%.

摘要

普拉德-威利综合征(PWS)是一种由多种不同遗传机制引起的神经行为障碍。所有这些机制都涉及15号染色体长臂1区1带至1区3带(15q11q13)上父源基因表达的缺失。尽管大多数PWS病例是散发性的,但由于复发风险因所涉及的机制而异,因此精确阐明致病遗传机制对于准确的遗传咨询至关重要。本文描述了一对受PWS影响的兄弟姐妹。两人在15q11q13区域均未发现显微镜下可见的缺失,也没有母源二体现象。对D15S63和小核核糖核蛋白多肽N(SNRPN)基因座的甲基化研究证实了PWS的诊断。分子研究显示,除了D15S128和D15S63这两个不存在父源贡献的区域表明印记中心缺失外,这对兄弟姐妹均表现为双亲遗传。家族研究表明,这对兄弟姐妹的父亲携带该缺失,且此缺失是他从母亲那里遗传而来的。他的后代患PWS的复发风险为50%。

相似文献

8
A case of Prader-Willi syndrome arising as a result of familial unbalanced translocation t(11;15)(q25;q13).
Clin Genet. 1998 Jul;54(1):60-4. doi: 10.1111/j.1399-0004.1998.tb03695.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验