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当喂养困难由遗传因素导致时:家族性部分9号染色体长臂重复的病例

When Feeding Difficulties Are due to Genetics: The Case of Familial Partial 9q Duplication.

作者信息

Travan Laura, Rocca Maria Santa, Buonomo Francesca, Cleva Lisa, Pecile Vanna, De Cunto Angela

机构信息

Institute for Maternal and Child Health, IRCCS "Burlo Garofolo", Trieste, Italy.

出版信息

J Investig Med High Impact Case Rep. 2015 Feb 18;3(1):2324709615574949. doi: 10.1177/2324709615574949. eCollection 2015 Jan-Mar.

Abstract

Chromosomal abnormalities may cause growth failure before or since birth. 9q duplication is reported as a cause of intrauterine growth restriction, mild dysmporphism, and intellectual disabilities. We report a case of a maternally inherited 9q21.31q21.33 duplication causing prenatal and postnatal growth restriction with feeding refusal and mild facial dysmorphisms, prenatally diagnosed by single-nucleotide polymorphism array analysis. Hypothesis of the possible pathogenic mechanisms are discussed.

摘要

染色体异常可能在出生前或出生后导致生长发育迟缓。据报道,9q重复是宫内生长受限、轻度畸形和智力障碍的一个原因。我们报告一例由母亲遗传的9q21.31q21.33重复导致的病例,该病例引起产前和产后生长受限、拒食以及轻度面部畸形,通过单核苷酸多态性阵列分析进行产前诊断。文中还讨论了可能的致病机制假说。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/420a/4586914/96422db5ceb2/10.1177_2324709615574949-fig1.jpg

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