Cargando…
Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient
Congenital insensitivity to pain with anhidrosis is a rare disease of the nervous system which causes one to lose his/her feeling of pain. The disease is subtype four of hereditary sensory and autonomic neuropathy (HSAN IV) that results from NTRK1 gene defect. Direct sequencing was performed to scre...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Neuroscience Society
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202553/ https://www.ncbi.nlm.nih.gov/pubmed/25337332 |
_version_ | 1782340309667020800 |
---|---|
author | Saleh-gohari, Nasrollah Mohammadi-Anaie, Marzye |
author_facet | Saleh-gohari, Nasrollah Mohammadi-Anaie, Marzye |
author_sort | Saleh-gohari, Nasrollah |
collection | PubMed |
description | Congenital insensitivity to pain with anhidrosis is a rare disease of the nervous system which causes one to lose his/her feeling of pain. The disease is subtype four of hereditary sensory and autonomic neuropathy (HSAN IV) that results from NTRK1 gene defect. Direct sequencing was performed to screen NTRK1 for mutations. The result revealed a homozygous deletion of adenine on intron 14 that may cause the disease. |
format | Online Article Text |
id | pubmed-4202553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Iranian Neuroscience Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42025532014-10-21 Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient Saleh-gohari, Nasrollah Mohammadi-Anaie, Marzye Basic Clin Neurosci Case Report Congenital insensitivity to pain with anhidrosis is a rare disease of the nervous system which causes one to lose his/her feeling of pain. The disease is subtype four of hereditary sensory and autonomic neuropathy (HSAN IV) that results from NTRK1 gene defect. Direct sequencing was performed to screen NTRK1 for mutations. The result revealed a homozygous deletion of adenine on intron 14 that may cause the disease. Iranian Neuroscience Society 2013 /pmc/articles/PMC4202553/ /pubmed/25337332 Text en Copyright © 2013 Iranian Neuroscience Society http://creativecommons.org/licenses/by-nc/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Case Report Saleh-gohari, Nasrollah Mohammadi-Anaie, Marzye Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient |
title | Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient |
title_full | Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient |
title_fullStr | Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient |
title_full_unstemmed | Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient |
title_short | Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient |
title_sort | congenital insensitivity to pain with anhidrosis in an iranian patient |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202553/ https://www.ncbi.nlm.nih.gov/pubmed/25337332 |
work_keys_str_mv | AT salehgoharinasrollah congenitalinsensitivitytopainwithanhidrosisinaniranianpatient AT mohammadianaiemarzye congenitalinsensitivitytopainwithanhidrosisinaniranianpatient |