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肯尼综合征:病例报告与文献综述

Kenny syndrome: case report and literature review.

作者信息

Tsai C E, Chiu P C, Lee M L

机构信息

Center of Medical Genetics. Tzu-Chi Buddhist General Hospital, Hua-Lien, Taiwan, ROC.

出版信息

J Formos Med Assoc. 1996 Oct;95(10):793-7.

PMID:8961678
Abstract

A 34-month-old girl presented with a clinical picture of Kenny syndrome. The clinical manisfestations included growth retardation, persistent open anterior fontanelle, prominent forehead, mid-facial dysplasia, hypocalcemic tetany and characteristic radiologic skeletal abnormalities. Serum levels of immunoreactive parathyroid hormone (PTH) remained inappropriately low during hypocalcemic episodes in the neonatal period; indicating that hypocalcemia was a consequence of the hypoparathyroid state. This is the first reported case of Kenny syndrome in Taiwan. The literature on the pathogenesis, etiology and genetic basis of this disorder is reviewed in this paper.

摘要

一名34个月大的女童表现出肯尼综合征的临床症状。临床表现包括生长发育迟缓、前囟持续开放、前额突出、面中部发育不良、低钙性手足搐搦以及特征性的放射学骨骼异常。新生儿期低钙血症发作时,血清免疫反应性甲状旁腺激素(PTH)水平仍异常偏低;这表明低钙血症是甲状旁腺功能减退状态的结果。这是台湾地区首例报道的肯尼综合征病例。本文对该疾病的发病机制、病因及遗传基础的文献进行了综述。

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