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13号染色体部分三体的核型-表型相关性。一例源于母亲染色体易位的病例报告。

Karyotype-phenotype correlation in partial trisomy 13. Report of a case due to maternal translocation.

作者信息

Bonioli E, Crisalli M, Monteverde R, Vianello M G

出版信息

Am J Dis Child. 1981 Dec;135(12):1115-7. doi: 10.1001/archpedi.1981.02130360023009.

Abstract

A partial trisomy 13q, originating from a maternal translocation, 46,XX,t(3;13) (p26;q22), occurred in a 3-month-old infant, affected by multiple congenital anomalies. A review of the previously reported cases of partial trisomy for the distal segment of the long arm of chromosome 13 is conclusive for the existence of a distinct clinical entity; however, it is difficult to assign particular malformations to specific chromosome bands.

摘要

一名3个月大的婴儿出现源自母亲染色体易位46,XX,t(3;13)(p26;q22)的13q部分三体,该婴儿患有多种先天性异常。对先前报道的13号染色体长臂远端部分三体病例的回顾证实存在一种独特的临床实体;然而,很难将特定的畸形归因于特定的染色体带。

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