Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited

First described in 1932 by Dearborn as ‘congenital pure analgesia’, congenital insensitivity to pain and anhydrosis (CIPA) or hereditary sensory and autonomic neuropathy (HSAN) type IV is an extremely rare autosomal recessive disorder. A 7-year-old female child who is an established case of congenit...

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Autores principales: Ravichandra, KS, Kandregula, Chaitanya Ram, Koya, Srikanth, Lakhotia, Disha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472877/
https://www.ncbi.nlm.nih.gov/pubmed/26124587
http://dx.doi.org/10.5005/jp-journals-10005-1288
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author Ravichandra, KS
Kandregula, Chaitanya Ram
Koya, Srikanth
Lakhotia, Disha
author_facet Ravichandra, KS
Kandregula, Chaitanya Ram
Koya, Srikanth
Lakhotia, Disha
author_sort Ravichandra, KS
collection PubMed
description First described in 1932 by Dearborn as ‘congenital pure analgesia’, congenital insensitivity to pain and anhydrosis (CIPA) or hereditary sensory and autonomic neuropathy (HSAN) type IV is an extremely rare autosomal recessive disorder. A 7-year-old female child who is an established case of congenital insensitivity to pain and anhydrosis visited the department of pediatric medicine with osteoarthritic neuropathy. A multidisciplinary team approach was utilized to treat the child under general anesthesia. This article also discusses the diagnostic and therapeutic dilemmas involved in treating this type of children. How to cite this article: Ravichandra KS, Kandregula CR, Koya S, Lakhotia D. Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited. Int J Clin Pediatr Dent 2015;8(1):75-81.
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spelling pubmed-44728772015-06-29 Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited Ravichandra, KS Kandregula, Chaitanya Ram Koya, Srikanth Lakhotia, Disha Int J Clin Pediatr Dent Case Report First described in 1932 by Dearborn as ‘congenital pure analgesia’, congenital insensitivity to pain and anhydrosis (CIPA) or hereditary sensory and autonomic neuropathy (HSAN) type IV is an extremely rare autosomal recessive disorder. A 7-year-old female child who is an established case of congenital insensitivity to pain and anhydrosis visited the department of pediatric medicine with osteoarthritic neuropathy. A multidisciplinary team approach was utilized to treat the child under general anesthesia. This article also discusses the diagnostic and therapeutic dilemmas involved in treating this type of children. How to cite this article: Ravichandra KS, Kandregula CR, Koya S, Lakhotia D. Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited. Int J Clin Pediatr Dent 2015;8(1):75-81. Jaypee Brothers Medical Publishers 2015 2015-04-28 /pmc/articles/PMC4472877/ /pubmed/26124587 http://dx.doi.org/10.5005/jp-journals-10005-1288 Text en Copyright © 2015; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Case Report
Ravichandra, KS
Kandregula, Chaitanya Ram
Koya, Srikanth
Lakhotia, Disha
Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited
title Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited
title_full Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited
title_fullStr Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited
title_full_unstemmed Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited
title_short Congenital Insensitivity to Pain and Anhydrosis: Diagnostic and Therapeutic Dilemmas revisited
title_sort congenital insensitivity to pain and anhydrosis: diagnostic and therapeutic dilemmas revisited
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472877/
https://www.ncbi.nlm.nih.gov/pubmed/26124587
http://dx.doi.org/10.5005/jp-journals-10005-1288
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