Leventhal L J, Straka P C, Schumacher H R
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia.
J Rheumatol. 1989 Sep;16(9):1274-7.
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.
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。
