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再探毛发-鼻-指(趾)综合征

The tricho-rhino-phalangeal syndrome revisited.

作者信息

Parizel P M, Dumon J, Vossen P, Rigaux A, De Schepper A M

出版信息

Eur J Radiol. 1987 May;7(2):154-6.

PMID:3496219
Abstract

The tricho-rhino-phalangeal syndrome (TRPS) is a rare congenital disorder, characterized by (1) a peculiar and somewhat pear-shaped nose, (2) sparse and brittle scalp hair, and (3) radiographic evidence of cone-shaped epiphyses of the hands. On the basis of clinical, radiographic and genetic criteria, two subtypes (type I and II) are discerned. We describe an intermediate "hybrid" variant of the TRPS in a patient with clinical and radiographic features of TRPS type I, but with a clearly abnormal karyotype, consistent with TRPS type II. The radiographic findings of the syndrome are reviewed, with particular emphasis on the cone-shaped epiphyses in the hands, the changes in the coxo-femoral joints and the atypical appearance of the pubic symphysis.

摘要

毛发-鼻-指综合征(TRPS)是一种罕见的先天性疾病,其特征为:(1)独特的、有点梨形的鼻子;(2)头皮毛发稀疏且脆弱;(3)手部骨骺呈锥形的影像学证据。根据临床、影像学和遗传学标准,可区分出两种亚型(I型和II型)。我们描述了一名TRPS的中间“混合”变体患者,其具有I型TRPS的临床和影像学特征,但核型明显异常,与II型TRPS一致。本文回顾了该综合征的影像学表现,特别强调了手部的锥形骨骺、髋股关节的变化以及耻骨联合的非典型外观。

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