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两姐妹患限制性皮肤病。

Restrictive dermopathy in two sisters.

作者信息

Hou Jia-Woei, Mai Chien-Fang

机构信息

Division of Medical Genetics, Department of Pediatrics, Chang Gung Children's Hospital, Taipei, Taiwan, ROC.

出版信息

Chang Gung Med J. 2003 Jul;26(7):510-4.

Abstract

Restrictive dermopathy (RD) is a very rare and lethal congenital skin disease. It is inherited by an autosomal recessive pattern with characteristic features of abnormally rigid skin, generalized joint contractures (arthrogryposis), and dysmorphic facies consisting of downward slanting eyes, a small pinched nose, low-set ears, a fixed open mouth in the O-position, and micrognathia. We report on 2 siblings from consecutive pregnancies affected with RD. They died of possible sepsis and respiratory insufficiency at 6 and 8 days after birth, respectively. This kind of stiff skin defect may lead to a fetal akinesia/hypokinesia deformation sequence, which causes the facial abnormalities of RD, as presented in these cases.

摘要

限制性皮肤病(RD)是一种非常罕见且致命的先天性皮肤病。它以常染色体隐性模式遗传,具有皮肤异常僵硬、全身性关节挛缩(关节弯曲)以及由向下倾斜的眼睛、小而尖的鼻子、低位耳朵、呈O形的固定开口嘴和小颌畸形组成的畸形面容等特征。我们报告了连续两胎受RD影响的2名兄弟姐妹。他们分别在出生后6天和8天死于可能的败血症和呼吸功能不全。这种皮肤僵硬缺陷可能导致胎儿运动不能/运动减少变形序列,从而引起如这些病例中所呈现的RD面部异常。

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