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泪腺-耳-齿-指综合征:下肢受累及严重先天性肾脏异常的证据

Lacrimo-auriculo-dento-digital syndrome: evidence for lower limb involvement and severe congenital renal anomalies.

作者信息

Bamforth J S, Kaurah P

机构信息

Department of Pediatrics, University of Alberta, Edmonton, Canada.

出版信息

Am J Med Genet. 1992 Aug 1;43(6):932-7. doi: 10.1002/ajmg.1320430605.

Abstract

We describe a 3-generation family with lacrimo-auriculo-dento-digital syndrome (LADD). In addition to the well described abnormalities of ears, teeth, lacrimal apparatus and digits, the patients exhibit several previously undescribed anomalies, including minor facial anomalies (broad forehead, telecanthus, bulbous nasal tip, full jaw, ptosis and flared nostrils), involvement of the first and second toes, and congenital renal disease causing death in the neonatal period in 2 cases.

摘要

我们描述了一个患有泪腺-耳-牙-指综合征(LADD)的三代家族。除了耳部、牙齿、泪器和手指的典型异常外,患者还表现出一些先前未描述的异常,包括轻微面部异常(宽额头、内眦距增宽、鼻尖球样、下颌饱满、上睑下垂和鼻孔外翻)、第一和第二趾受累,以及2例导致新生儿期死亡的先天性肾病。

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