Narayanan V
Maxillofacial Unit, St Luke's Hospital, Bradford, UK.
Br J Oral Maxillofac Surg. 1996 Oct;34(5):446-9. doi: 10.1016/s0266-4356(96)90105-9.
Hereditary sensory neuropathies are a rare group of neurological disorders manifested from early childhood by diminished or absent sensibility to pain, touch and temperature. A Kashmiri family with four members affected by congenital sensory neuropathy and its oral manifestations is described. Pain and temperature sensation was lost in various parts of the body including the orofacial region resulting in mutilating acropathy, particularly of the limbs and face. Orofacial motor function was normal. Three of the four members had corneal opacification due to scarring from keratitis. To prevent any further mutilation, any corrective surgery is best delayed until the patient is old enough. A discussion of the oral manifestations of this condition with a review of the literature is presented.
遗传性感觉神经病是一组罕见的神经系统疾病,从幼儿期开始就表现为对疼痛、触觉和温度的感觉减退或丧失。本文描述了一个克什米尔家庭,其中四名成员患有先天性感觉神经病及其口腔表现。身体的各个部位,包括口面部区域,都失去了痛觉和温度觉,导致肢体残毁性病变,尤其是四肢和面部。口面部运动功能正常。四名成员中有三名因角膜炎瘢痕形成而出现角膜混浊。为防止进一步的肢体残毁,任何矫正手术最好推迟到患者年龄足够大时进行。本文对该疾病的口腔表现进行了讨论,并对相关文献进行了综述。