哈伊杜－切尼综合征：一例病例报告及文献综述
The Hajdu-Cheney syndrome: a case report and review of the literature.
作者信息
Diren H B, Kovanlikaya I, Süller A, Dicle O
机构信息
Department of Radiology, Dokuz Eylül University, Faculty of Medicine, Izmir, Turkey.
出版信息
Pediatr Radiol. 1990;20(7):568-9. doi: 10.1007/BF02011397.
PMID:2216599
Abstract
Hajdu-Cheney syndrome which is also known as type VI idiopathic osteolysis is a rare disease transmitted autosomal dominantly. In this syndrome, osteolysis involves primarily the terminal phalanges. We describe here a 18-year-old boy with typical clinical and radiological signs of Hajdu-Cheney syndrome.
摘要
哈伊杜-切尼综合征，也称为VI型特发性骨质溶解症，是一种罕见的常染色体显性遗传病。在这种综合征中，骨质溶解主要累及指骨末端。我们在此描述一名18岁男孩，具有典型的哈伊杜-切尼综合征临床和放射学征象。
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