II型原始小头畸形侏儒症。报告一例生长完全的患者]。

Annales de pediatrie Pub Date : 1993-05-01
D Théau, P Maroteaux
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引用次数: 0

摘要

II型原始小头侏儒症是一种罕见的鸟头侏儒症,于1982年由Majewski个体化。1例发育完全的女性患者表现出主要特征,包括产前发病时严重发育迟缓(身高降低4个标准差以上),四肢短,髋外翻伴髋骺端松解,干骺端膨大,在某些情况下,尺骨短,桡骨弯曲。很可能是遗传原因(常染色体隐性遗传)。本文报道的病例的许多特征可能与发病相关:骨骺闭合前生长激素水平升高,之后正常,青春期没有生长突增,青春期后多囊卵巢伴多毛,手术伤口愈合异常缓慢。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Type II primordial microcephalic dwarfism. Report of a patient with completed growth].

Type II primordial microcephalic dwarfism is a rare form of bird-headed dwarfism individualized in 1982 by Majewski. A case in a female patent with completed growth illustrates the main features, which include severe growth retardation (greater than 4 SD reduction in height) of prenatal onset, short limbs, coxa vara with epiphysiolysis of the hips, metaphyseal flaring and, in some instances, shortness of the ulnas and curvature of the radiuses. A genetic cause (with autosomal recessive inheritance) is very likely. A number of features in the case reported herein may be of pathogenetic relevance: growth hormone levels were elevated before closure of the epiphyses and normal thereafter, no growth spurt occurred at puberty, polycystic ovaries with hirsutism developed after puberty, and surgical wound healing was unusually slow.

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