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扩大ADNP相关疾病的范围——产前诊断的先天性膈疝与ADNP基因的一种新的新发突变

Expanding the spectrum of ADNP-related disorder-Antenatally diagnosed congenital diaphragmatic hernia and a novel de novo mutation in ADNP gene.

作者信息

Asegaonkar Prashant, Kotecha Udhaya, Dongre Mayuresh, Mistri Mehul, Sharda Sheetal

机构信息

Garbhankur Fetal Medicine Centre, Aurangabad, India.

Neuberg Centre for Genomic Medicine, Ahmedabad, India.

出版信息

Am J Med Genet A. 2023 Jan;191(1):275-279. doi: 10.1002/ajmg.a.63017. Epub 2022 Nov 2.

Abstract

De novo heterozygous ADNP variants have been associated with a complex neurological phenotype characterized primarily by neurodevelopmental delay. Cardiac and renal anomalies have additionally been observed in a few patients. All reported cases to date have been ascertained postnatally. Congenital diaphragmatic hernia (CDH) has been previously observed in one child diagnosed with a de novo ADNP-related neurodevelopmental disorder. We report a fetus who presented with syndromic CDH associated with a de novo heterozygous ADNP variant.

摘要

新生杂合性ADNP变异与一种主要以神经发育迟缓为特征的复杂神经学表型相关。少数患者还观察到心脏和肾脏异常。迄今为止,所有报告的病例都是在出生后确诊的。先天性膈疝(CDH)此前曾在一名被诊断患有新生ADNP相关神经发育障碍的儿童中观察到。我们报告了一名患有综合征性CDH并伴有新生杂合性ADNP变异的胎儿。

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