Literature DB >> 27042602

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

Neena Indavara Eregowda1, Sneha Yadav2, Poornima Parameshwarappa3, Roopa Korishettar Basavraj1.   

Abstract

Entities:  

Keywords:  Anhidrosis; Congenital insensitivity to pain; Hereditary sensory autonomic neuropathy

Year:  2016        PMID： 27042602      PMCID： PMC4800669          DOI： 10.7860/JCDR/2016/16514.7317

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN： 0973-709X


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  7 in total

1.  Congenital sensory neuropathy with anhidrosis.

Authors:  L C Thakur; V Chandran; K S Anand
Journal:  Indian Pediatr       Date:  1992-08       Impact factor: 1.411

2.  Hereditary sensory autonomic neuropathy Type IV.

Authors:  Tarun Dua; Jyoti Sharma; Tanu Singhal; Ved Bhushan Arya
Journal:  Indian Pediatr       Date:  2005-03       Impact factor: 1.411

3.  Hereditary sensory and autonomic neuropathy type IV.

Authors:  Sunil Karande; Nitin Satam
Journal:  Indian Pediatr       Date:  2005-06       Impact factor: 1.411

4.  Congenital insensitivity to pain--review and report of a case with dental implications.

Authors:  Jonathan Butler; Padraig Fleming; David Webb
Journal:  Oral Surg Oral Med Oral Pathol Oral Radiol Endod       Date:  2005-11-11

Review 5.  Hereditary sensory and autonomic neuropathy: review and a case report with dental implications.

Authors:  T L Erdem; I Ozcan; D Ilgüy; S Sirin
Journal:  J Oral Rehabil       Date:  2000-02       Impact factor: 3.837

6.  Neurotrophic keratitis and congenital insensitivity to pain with anhidrosis--a case report with 10-year follow-up.

Authors:  Deepa John; Maya Thomas; Pushpa Jacob
Journal:  Cornea       Date:  2011-01       Impact factor: 2.651

7.  Congenital insensitivity to pain and anhidrosis: a case report from South India.

Authors:  Carounanidy Udayashankar; P Oudeacoumar; Amiya Kumar Nath
Journal:  Indian J Dermatol       Date:  2012-11       Impact factor: 1.494
  7 in total
  2 in total

Review 1.  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

2.  Congenital Insensitivity to Pain with Anhidrosis: A Rare Entity.

Authors:  Priya Rajbansh; Mamta Yadav; Piyush Kumar; Anupam Das
Journal:  Indian Dermatol Online J       Date:  2020-03-09
  2 in total

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