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先天性胫骨前外侧弓形弯曲并多指畸形:一例报告

Congenital anterolateral tibial bowing and polydactyly: a case report.

作者信息

Lemire Edmond G

机构信息

Division of Medical Genetics, Department of Pediatrics, University of Saskatchewan, Saskatoon, SK, S7N 0W8, Canada.

出版信息

J Med Case Rep. 2007 Jul 23;1:54. doi: 10.1186/1752-1947-1-54.

Abstract

Congenital anterolateral bowing of the tibia is a rare deformity that may lead to pseudarthrosis and risk of fracture. This is commonly associated with neurofibromatosis type 1. In this report, we describe a 15-month old male with congenital anterolateral bowing of the right tibia and associated hallux duplication. This is a distinct entity with a generally favourable prognosis that should not be confused with other conditions such as neurofibromatosis type 1. Previously published cases are reviewed.

摘要

先天性胫骨前外侧弓形弯曲是一种罕见的畸形,可能导致假关节形成和骨折风险。这通常与1型神经纤维瘤病相关。在本报告中,我们描述了一名15个月大的男性,患有右胫骨先天性前外侧弓形弯曲并伴有拇趾重复畸形。这是一种具有总体良好预后的独特病症,不应与其他病症如1型神经纤维瘤病相混淆。我们回顾了先前发表的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c35/1948010/3a46331f423e/1752-1947-1-54-1.jpg

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