Literature DB >> 8909740

Oral and maxillofacial manifestations of hereditary sensory neuropathy.

V Narayanan1.   

Abstract

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.

Entities:  

Mesh:

Year:  1996        PMID: 8909740     DOI: 10.1016/s0266-4356(96)90105-9

Source DB:  PubMed          Journal:  Br J Oral Maxillofac Surg        ISSN: 0266-4356            Impact factor:   1.651


  3 in total

1.  Hereditary sensory and autonomic neuropathy type V: Report of a rare case.

Authors:  Ritesh Kalaskar; Ashita Kalaskar
Journal:  Contemp Clin Dent       Date:  2015 Jan-Mar

2.  Congenital Insensitivity to Pain and Anhydrosis (CIPA) Syndrome; A Report of 4 Cases.

Authors:  Khadije Daneshjou; Hanieh Jafarieh; Seyed-Reza Raaeskarami
Journal:  Iran J Pediatr       Date:  2012-09       Impact factor: 0.364

3.  Congenital Insensitivity to Pain without Anhidrosis: Orodental Problems and Management.

Authors:  N Abdullah; Kausar Sadia Fakhruddin; A R Samsudin
Journal:  Case Rep Dent       Date:  2015-09-20
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.