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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...

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Autores principales: de Almeida Jr., Hiram Larangeira, Garcias, Gilberto, Silva, Ricardo Marques e, Batista, Stela Laner, Pasetto, Fernanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2016
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.
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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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