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南非关节挛缩综合征的诊断考量

Diagnostic considerations in arthrogryposis syndromes in South Africa.

作者信息

Gericke G S, Hall J G, Nelson M M, Beighton P H

出版信息

Clin Genet. 1984 Feb;25(2):155-62.

PMID:6538466
Abstract

Congenital rigidity of multiple joints poses a difficult diagnostic and therapeutic problem. There are also semantic difficulties as the non-specific term "arthrogryposis" is often used for any individual with congenital limitation of joint movement. Many distinct syndromes present in this way and as they differ in their course, prognosis and genetic implications, diagnostic precision is crucial. A diagnostic analysis is given of 247 South African patients in whom "arthrogryposis" had been recorded, and the pathogenesis and nosology of congenital contractures are discussed in this paper. Three of these stiff joint conditions were originally described in South African patients, i.e. Liebenberg synostosis syndrome, digitotalar dysmorphism, and the Gordon syndrome of autosomal dominant cleft palate, camptodactyly and club feet.

摘要

先天性多关节僵硬是一个诊断和治疗难题。此外,语义上也存在困难,因为非特异性术语“关节挛缩症”常被用于任何有先天性关节活动受限的个体。许多不同的综合征都以这种方式呈现,由于它们在病程、预后和遗传意义上存在差异,诊断的精确性至关重要。本文对247例记录有“关节挛缩症”的南非患者进行了诊断分析,并讨论了先天性挛缩的发病机制和疾病分类。其中三种关节僵硬病症最初是在南非患者中描述的,即利本伯格骨连接综合征、指距骨畸形以及常染色体显性腭裂、屈曲指和马蹄内翻足的戈登综合征。

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