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遗传性感觉和自主神经病变:综述及1例具有牙科意义的病例报告

Hereditary sensory and autonomic neuropathy: review and a case report with dental implications.

作者信息

Erdem T L, Ozcan I, Ilgüy D, Sirin S

机构信息

Faculty of Dentistry, Department of Oral Diagnosis and Radiology, University of Istanbul, Istanbul, Turkey.

出版信息

J Oral Rehabil. 2000 Feb;27(2):180-3. doi: 10.1046/j.1365-2842.2000.00474.x.

Abstract

Hereditary sensory and autonomic neuropathy (HSAN) is a rare syndrome which is seen in early childhood. Five different types are described. Absence of pain and self-mutilation are characteristic findings of this syndrome. Teeth in the oral cavity can cause damage to the oral tissues and tongue. When it is diagnosed, there should be co-operation between dentist and neurologist. Using an oral shield prevents the biting and, thus, traumatization of the tissues can be prevented. A case report which is diagnosed as HSAN type 4 is presented and information submitted about its treatment.

摘要

遗传性感觉和自主神经病变(HSAN)是一种罕见的综合征,多见于儿童早期。该综合征有五种不同类型。无痛觉和自残行为是此综合征的典型表现。口腔内的牙齿会对口腔组织和舌头造成损伤。确诊后,牙医和神经科医生应相互协作。使用口腔防护装置可防止咬伤,从而避免组织受到创伤。本文报告了一例被诊断为4型HSAN的病例,并提供了相关治疗信息。

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