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Pili canaliculi as manifestation of giant axonal neuropathy
Giant axonal neuropathy is a rare autosomal recessive neurodegenerative disease. The condition is characterized by neurons with abnormally large axons due to intracellular filament accumulation. The swollen axons affect both the peripheral and central nervous system. A 6-year old female patient had...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Dermatologia
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325017/ https://www.ncbi.nlm.nih.gov/pubmed/28300918 http://dx.doi.org/10.1590/abd1806-4841.20164677 |
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author | de Almeida Jr., Hiram Larangeira Garcias, Gilberto Silva, Ricardo Marques e Batista, Stela Laner Pasetto, Fernanda |
author_facet | de Almeida Jr., Hiram Larangeira Garcias, Gilberto Silva, Ricardo Marques e Batista, Stela Laner Pasetto, Fernanda |
author_sort | de Almeida Jr., Hiram Larangeira |
collection | PubMed |
description | Giant axonal neuropathy is a rare autosomal recessive neurodegenerative disease. The condition is characterized by neurons with abnormally large axons due to intracellular filament accumulation. The swollen axons affect both the peripheral and central nervous system. A 6-year old female patient had been referred to a geneticist reporting problems with walking and hypotonia. At the age of 10, she became wheelchair dependent. Scanning electron microscopy of a curly hair classified it as pili canaliculi. GAN gene sequencing demonstrated mutation c.1456G>A (p.GLU486LYS). At the age of 12, the patient died due to respiratory complications. Dermatologists should be aware of this entity since hair changes are considered suggestive of GAN. |
format | Online Article Text |
id | pubmed-5325017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Sociedade Brasileira de Dermatologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-53250172017-03-02 Pili canaliculi as manifestation of giant axonal neuropathy de Almeida Jr., Hiram Larangeira Garcias, Gilberto Silva, Ricardo Marques e Batista, Stela Laner Pasetto, Fernanda An Bras Dermatol Case Report Giant axonal neuropathy is a rare autosomal recessive neurodegenerative disease. The condition is characterized by neurons with abnormally large axons due to intracellular filament accumulation. The swollen axons affect both the peripheral and central nervous system. A 6-year old female patient had been referred to a geneticist reporting problems with walking and hypotonia. At the age of 10, she became wheelchair dependent. Scanning electron microscopy of a curly hair classified it as pili canaliculi. GAN gene sequencing demonstrated mutation c.1456G>A (p.GLU486LYS). At the age of 12, the patient died due to respiratory complications. Dermatologists should be aware of this entity since hair changes are considered suggestive of GAN. Sociedade Brasileira de Dermatologia 2016 /pmc/articles/PMC5325017/ /pubmed/28300918 http://dx.doi.org/10.1590/abd1806-4841.20164677 Text en http://creativecommons.org/licenses/by/4.0/ 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 de Almeida Jr., Hiram Larangeira Garcias, Gilberto Silva, Ricardo Marques e Batista, Stela Laner Pasetto, Fernanda Pili canaliculi as manifestation of giant axonal neuropathy |
title | Pili canaliculi as manifestation of giant axonal neuropathy |
title_full | Pili canaliculi as manifestation of giant axonal neuropathy |
title_fullStr | Pili canaliculi as manifestation of giant axonal neuropathy |
title_full_unstemmed | Pili canaliculi as manifestation of giant axonal neuropathy |
title_short | Pili canaliculi as manifestation of giant axonal neuropathy |
title_sort | pili canaliculi as manifestation of giant axonal neuropathy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325017/ https://www.ncbi.nlm.nih.gov/pubmed/28300918 http://dx.doi.org/10.1590/abd1806-4841.20164677 |
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