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短肋综合征——比默尔型(同胞兄妹)。

Short rib syndrome--Beemer type in sibs.

作者信息

Hennekam R C

机构信息

Clinical Genetics Center Utrecht, The Netherlands.

出版信息

Am J Med Genet. 1991 Aug 1;40(2):230-3. doi: 10.1002/ajmg.1320400221.

Abstract

The short rib (polydactyly) syndrome Beemer type is a rare lethal osteochondrodysplasia characterized clinically by short limbs, median cleft upper lip and palate, narrow thorax, and protuberant abdomen, and radiologically by short ribs, short and bowed long bones, and mild platyspondyly. Two affected female sibs are described, one having a preaxial polydactyly of the feet. The differentiation with the short rib syndrome Majewski type relies mainly on the radiological appearance of the tibia. Molecular biology may eventually prove whether the 2 conditions are truly separate entities or not.

摘要

短肋(多指)综合征比默尔型是一种罕见的致死性骨软骨发育不良,临床特征为四肢短小、上唇和上颚正中裂、胸廓狭窄和腹部突出,放射学特征为短肋、短而弯曲的长骨以及轻度椎体扁平。本文描述了两名患病女性同胞,其中一人足部有轴前多指。与马耶夫斯基型短肋综合征的鉴别主要依靠胫骨的放射学表现。分子生物学最终可能会证明这两种情况是否真的是独立的实体。

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