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Congenital insensitivity to pain with anhydrosis: report of a family case
Congenital Insensitivity to pain with anhydrosis (CIPA) is a rare inherited disease. It is classified as hereditary sensory and autonomic neuropathy type IV. Pain insensitivity and autonomic deficits are present, but touch and pressure sensitivity are unimpaired. Mental retardation is usually presen...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215555/ https://www.ncbi.nlm.nih.gov/pubmed/22355435 |
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author | Labib, Smael Adnane Berdai, Mohamed Abourazzak, Sanae Hida, Mustapha Harandou, Mustapha |
author_facet | Labib, Smael Adnane Berdai, Mohamed Abourazzak, Sanae Hida, Mustapha Harandou, Mustapha |
author_sort | Labib, Smael |
collection | PubMed |
description | Congenital Insensitivity to pain with anhydrosis (CIPA) is a rare inherited disease. It is classified as hereditary sensory and autonomic neuropathy type IV. Pain insensitivity and autonomic deficits are present, but touch and pressure sensitivity are unimpaired. Mental retardation is usually present. We report a family case of a 5 years old girl and 2 years old boy with congenital insensitivity to pain, while discussing the clinical features and the anesthetic strategy of such patients. Patients with Congenital Insensitivity to Pain with anhydrosis may undergo surgery because of susceptibility to trauma due to absence of pain. The clinical features may intrinsically possess anesthetic challenges. |
format | Online Article Text |
id | pubmed-3215555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-32155552012-02-21 Congenital insensitivity to pain with anhydrosis: report of a family case Labib, Smael Adnane Berdai, Mohamed Abourazzak, Sanae Hida, Mustapha Harandou, Mustapha Pan Afr Med J Case Report Congenital Insensitivity to pain with anhydrosis (CIPA) is a rare inherited disease. It is classified as hereditary sensory and autonomic neuropathy type IV. Pain insensitivity and autonomic deficits are present, but touch and pressure sensitivity are unimpaired. Mental retardation is usually present. We report a family case of a 5 years old girl and 2 years old boy with congenital insensitivity to pain, while discussing the clinical features and the anesthetic strategy of such patients. Patients with Congenital Insensitivity to Pain with anhydrosis may undergo surgery because of susceptibility to trauma due to absence of pain. The clinical features may intrinsically possess anesthetic challenges. The African Field Epidemiology Network 2011-07-25 /pmc/articles/PMC3215555/ /pubmed/22355435 Text en © Smael Labib et al. http://creativecommons.org/licenses/by/2.0 The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Labib, Smael Adnane Berdai, Mohamed Abourazzak, Sanae Hida, Mustapha Harandou, Mustapha Congenital insensitivity to pain with anhydrosis: report of a family case |
title | Congenital insensitivity to pain with anhydrosis: report of a family case |
title_full | Congenital insensitivity to pain with anhydrosis: report of a family case |
title_fullStr | Congenital insensitivity to pain with anhydrosis: report of a family case |
title_full_unstemmed | Congenital insensitivity to pain with anhydrosis: report of a family case |
title_short | Congenital insensitivity to pain with anhydrosis: report of a family case |
title_sort | congenital insensitivity to pain with anhydrosis: report of a family case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3215555/ https://www.ncbi.nlm.nih.gov/pubmed/22355435 |
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