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1 级小耳畸形、宽额前囟和新型梅硫哒唑胚胎病气管食管瘘。

Grade 1 microtia, wide anterior fontanel and novel type tracheo-esophageal fistula in methimazole embryopathy.

机构信息

Division of Medical Genetics, A. I. duPont Hospital for Children, Wilmington, Delaware, USA.

出版信息

Am J Med Genet A. 2011 Mar;155A(3):526-33. doi: 10.1002/ajmg.a.33705. Epub 2011 Feb 22.

Abstract

Carbimazole (CMZ) and its active metabolite methimazole (MMI) are antithyroid medications, which can result in MMI/CMZ embryopathy in susceptible individuals. The incidence of birth defects related to MMI/CMZ embryopathy remains unclear as several epidemiologic studies failed to prove a correlation, despite positive case-control studies and numerous case reports. Malformations reported in exposed individuals and commonly recognized as MMI/CMZ embryopathy include cutis aplasia of the scalp, choanal atresia, esophageal atresia (EA), tracheo-esophageal fistula (TEF), persistent vitelline duct, athelia/hypothelia, and subtle facial dysmorphisms including sparse or arched eyebrows. Here, we report on individuals with early pregnancy exposure to MMI, with microtia and various other anomalies associated with MMI embryopathy, suggesting that microtia is also seen with increased frequency after prenatal MMI exposure. Additional unusual malformations among our patients include a previously unreported type of TEF with three separate esophageal pouches and a fistula connecting the middle pouch to the trachea in one child, and absence of the gall bladder in another. An enlarged anterior fontanel was seen in three patients, and clinodactyly of the fifth finger was noted in three. The similarities between our three patients with microtia after MMI exposure and the two previously reported with microtia after CMZ exposure support the concept of microtia being related to the MMI/CMZ exposure. Recognition of microtia as a manifestation of MMI/CMZ embryopathy will likely increase the number of diagnosed cases and thus affect ascertainment. We propose diagnostic criteria for MMI/CMZ embryopathy, including the presence of at least one major characteristic finding.

摘要

甲巯咪唑 (CMZ) 和其活性代谢物甲巯咪唑 (MMI) 是抗甲状腺药物,可导致易感个体发生 MMI/CMZ 胚胎病。与 MMI/CMZ 胚胎病相关的出生缺陷发生率尚不清楚,尽管有阳性病例对照研究和大量病例报告,但几项流行病学研究未能证明存在相关性。暴露个体中报告的畸形通常被认为是 MMI/CMZ 胚胎病,包括头皮皮肤发育不全、后鼻孔闭锁、食管闭锁 (EA)、气管食管瘘 (TEF)、持续性脐动脉、无眼/小眼和微妙的面部畸形,包括稀疏或拱形眉毛。在这里,我们报告了在妊娠早期接触 MMI 的个体,以及与 MMI 胚胎病相关的其他各种异常,表明在产前 MMI 暴露后,小耳畸形的发生频率也增加了。我们患者中的其他不寻常畸形包括一例以前未报道的 TEF,有三个独立的食管囊和一个连接中间囊和气管的瘘管,另一个孩子没有胆囊。三个患者前囟增大,三个患者第五指内弯。我们三个 MMI 暴露后出现小耳畸形的患者与两个以前报道的 CMZ 暴露后出现小耳畸形的患者相似,支持小耳畸形与 MMI/CMZ 暴露有关的概念。认识到小耳畸形是 MMI/CMZ 胚胎病的一种表现形式,可能会增加诊断病例的数量,从而影响确定。我们提出了 MMI/CMZ 胚胎病的诊断标准,包括至少有一个主要特征性发现。

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