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Early-onset Hirayama disease in a female
OBJECTIVES: Hirayama disease is a rare myelopathy, occurring predominantly in males with onset in the teens. METHODS AND RESULTS: Here, we report a young female patient who developed the first signs of Hirayama disease at 10.5 years of age. Prior to onset, she had experienced a growth spurt and grew...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308420/ https://www.ncbi.nlm.nih.gov/pubmed/28228960 http://dx.doi.org/10.1177/2050313X16686710 |
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author | Baumann, Matthias Finsterer, Josef Gizewski, Elke R Löscher, Wolfgang N |
author_facet | Baumann, Matthias Finsterer, Josef Gizewski, Elke R Löscher, Wolfgang N |
author_sort | Baumann, Matthias |
collection | PubMed |
description | OBJECTIVES: Hirayama disease is a rare myelopathy, occurring predominantly in males with onset in the teens. METHODS AND RESULTS: Here, we report a young female patient who developed the first signs of Hirayama disease at 10.5 years of age. Prior to onset, she had experienced a growth spurt and grew about 8 cm. The disease progressed over 3 years and the typical clinical, electrophysiological, and neuroimaging signs of Hirayama disease were found. After this period and achievement of her final height, no further progression was noticed. CONCLUSIONS: This case highlights that pediatric neurologists should be aware of Hirayama disease, which can also occur in girls in early adolescence. |
format | Online Article Text |
id | pubmed-5308420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-53084202017-02-22 Early-onset Hirayama disease in a female Baumann, Matthias Finsterer, Josef Gizewski, Elke R Löscher, Wolfgang N SAGE Open Med Case Rep Case Report OBJECTIVES: Hirayama disease is a rare myelopathy, occurring predominantly in males with onset in the teens. METHODS AND RESULTS: Here, we report a young female patient who developed the first signs of Hirayama disease at 10.5 years of age. Prior to onset, she had experienced a growth spurt and grew about 8 cm. The disease progressed over 3 years and the typical clinical, electrophysiological, and neuroimaging signs of Hirayama disease were found. After this period and achievement of her final height, no further progression was noticed. CONCLUSIONS: This case highlights that pediatric neurologists should be aware of Hirayama disease, which can also occur in girls in early adolescence. SAGE Publications 2017-01-01 /pmc/articles/PMC5308420/ /pubmed/28228960 http://dx.doi.org/10.1177/2050313X16686710 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Case Report Baumann, Matthias Finsterer, Josef Gizewski, Elke R Löscher, Wolfgang N Early-onset Hirayama disease in a female |
title | Early-onset Hirayama disease in a female |
title_full | Early-onset Hirayama disease in a female |
title_fullStr | Early-onset Hirayama disease in a female |
title_full_unstemmed | Early-onset Hirayama disease in a female |
title_short | Early-onset Hirayama disease in a female |
title_sort | early-onset hirayama disease in a female |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308420/ https://www.ncbi.nlm.nih.gov/pubmed/28228960 http://dx.doi.org/10.1177/2050313X16686710 |
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