Literature DB >> 10672155

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

T L Erdem1, I Ozcan, D Ilgüy, S Sirin.   

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.

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Year:  2000        PMID: 10672155     DOI: 10.1046/j.1365-2842.2000.00474.x

Source DB:  PubMed          Journal:  J Oral Rehabil        ISSN: 0305-182X            Impact factor:   3.837


  4 in total

1.  A Girl with No Pain: Congenital Insensitivity To Pain and Anhidrosis (HSAN) Type IV - A Case Report.

Authors:  Neena Indavara Eregowda; Sneha Yadav; Poornima Parameshwarappa; Roopa Korishettar Basavraj
Journal:  J Clin Diagn Res       Date:  2016-02-01

2.  Congenital Insensitivity to Pain with Anhidrosis (CIPA): A Case Report.

Authors:  A Safari; A A Khaledi; M Vojdani
Journal:  Iran Red Crescent Med J       Date:  2011-02-01       Impact factor: 0.611

Review 3.  Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.

Authors:  Karim Elhennawy; Seif Reda; Christian Finke; Luitgard Graul-Neumann; Paul-Georg Jost-Brinkmann; Theodosia Bartzela
Journal:  J Med Case Rep       Date:  2017-08-15

4.  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
  4 in total

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