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儿童期免疫失调、多内分泌腺病、肠病、X连锁综合征中的雅各布关节病和肢端骨质溶解症。

Jaccoud arthropathy and acroosteolysis in KID syndrome.

作者信息

Leventhal L J, Straka P C, Schumacher H R

机构信息

Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia.

出版信息

J Rheumatol. 1989 Sep;16(9):1274-7.

PMID:2810288
Abstract

KID (keratitis, ichthyosis, deafness) syndrome is a congenital ectodermal defect of unknown etiology. Although achilles tendon retraction has been seen on several occasions, no other evidence of skeletal, articular or enthesopathic processes has been described. We report a patient with KID syndrome and acroosteolytic changes on radiographs, along with clinical and radiographic evidence of Jaccoud arthropathy.

摘要

KID(角膜炎、鱼鳞病、耳聋)综合征是一种病因不明的先天性外胚层缺陷。虽然曾有几次观察到跟腱挛缩,但尚未有关于骨骼、关节或附着点病过程的其他证据的描述。我们报告了一名患有KID综合征的患者,其X线片显示有肢端骨质溶解改变,同时还有Jaccoud关节病的临床和影像学证据。

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