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18号染色体长臂增加,源自平衡易位t(1;18)mat的子代:尸检结果的病例报告

18q+, the progeny of a balanced translocation t(1;18)mat: case report with necropsy findings.

作者信息

Hindi A, Beneck D, Greco M A, Wolman S R

出版信息

J Med Genet. 1986 Jun;23(3):263-6. doi: 10.1136/jmg.23.3.263.

Abstract

A female infant with additional genetic material on the long arm of chromosome 18 is described. Cytogenetic studies of the infant and her mother showed that the altered region resulted from an unbalanced translocation of part of the long arm of chromosome 1. This chromosomal abnormality has not been reported previously, according to a recent registry of abnormal chromosome patterns. The patient had hydrops fetalis and multiple congenital abnormalities, involving the cardiovascular, respiratory, and skeletal systems, together with unusual facies. External features, radiological findings, and gross and microscopical examination at necropsy are presented and compared with previously reported cases of related but dissimilar chromosomal abnormalities.

摘要

本文描述了一名18号染色体长臂存在额外遗传物质的女婴。对该婴儿及其母亲的细胞遗传学研究表明,该改变区域是由1号染色体长臂部分的不平衡易位导致的。根据最近的异常染色体模式登记处的数据,这种染色体异常此前尚未有过报道。该患者患有胎儿水肿和多种先天性异常,累及心血管、呼吸和骨骼系统,同时伴有特殊面容。文中呈现了尸检时的外部特征、影像学检查结果以及大体和显微镜检查结果,并与之前报道的相关但不同的染色体异常病例进行了比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b683/1049641/d4bcefacd697/jmedgene00089-0072-a.jpg

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