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伴有严重营养和感觉障碍的夏科-马里-图思病。对一例长达半个世纪的病例进行的解剖学研究。

Charcot-Marie-Tooth's disease with severe trophic and sensory disorders. Study of a case following along a half a century with anatomical studies.

作者信息

Barraquer-Bordas L, Navarro C, Salisachs P

机构信息

Department of Neurology, Hospital de la Sta. Creu i Sant Pau, Valle de Hebrón, España.

出版信息

Acta Neurol Latinoam. 1981;27(3-4):177-89.

PMID:6965173
Abstract

Plantar ulcers of neurological origin are known to be associated with several disorders, some of which may be familial. We present the case report together with the clinical and post-mortem data of a patient with peroneal muscular atrophy of the Charcot-Marie-Tooth type and plantar ulcers as a prominent feature. At least three other members of her family had Charcot-Marie-Tooth disease. The family pedigree is included. The discussion stresses the difference between patients with Charcot-Marie-Tooth disease with associated manifestations, bony destruction of the feet and plantar ulcers and patients with hereditary motor and hereditary sensory radicular neuropathies.

摘要

已知神经源性足底溃疡与多种疾病相关,其中一些可能具有家族性。我们报告了一例以夏科-马里-图思型腓骨肌萎缩症和足底溃疡为突出特征的患者的病例报告,并附上临床和尸检数据。她的家族中至少还有其他三名成员患有夏科-马里-图思病。文中包含家族谱系。讨论强调了伴有相关表现、足部骨质破坏和足底溃疡的夏科-马里-图思病患者与遗传性运动和遗传性感觉神经根神经病患者之间的差异。

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