头胎胎儿马蹄内翻足:严重成骨不全症的一种新表现形式

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Chloe Barnett, Kaitlyn Eddy, Phillip N. Rauk, Jill Lewter
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引用次数: 0

摘要

马蹄内翻足(Talipes equinovarus),又称马蹄内翻足,是一种比较常见的先天性缺陷,大约每 1000 个活产婴儿中就有一个患有此病。大多数马蹄内翻足病例是特发性的,与潜在的遗传综合征无关。约有 20% 的病例可以确定有明确的遗传病因。这里我们介绍两例在妊娠头三个月通过胎儿超声发现的双侧马蹄内翻足,并在妊娠第二个三个月诊断为成骨不全症。两个胎儿均出现多发性骨折,并被鉴定为 COL1A1 功能缺失变异。据我们所知,妊娠头三个月出现足畸形与成骨不全症之间的关联以前从未报道过,这为及时诊断、遗传咨询和检测以及适当的管理提供了难得的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First Trimester Fetal Clubfoot: A Novel Presentation of Severe Osteogenesis Imperfecta
Talipes equinovarus, also called clubfoot, is a relatively common congenital defect affecting approximately one in every 1000 live births. Most cases of clubfoot are expected to be idiopathic and unrelated to an underlying genetic syndrome. In approximately 20% of cases, a clear genetic etiology is identified. Here we present two cases of bilateral clubfoot identified via fetal ultrasound in the first trimester associated with osteogenesis imperfecta diagnosed in the second trimester. Both fetuses presented with multiple fractures and were identified to have loss‐of‐function variants in COL1A1. An association between clubfeet in the first trimester and osteogenesis imperfecta has not been previously reported to the best of our knowledge, which leads to unique opportunities for prompt diagnosis, genetic counseling and testing, and appropriate management.
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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