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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...

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Autores principales: Baumann, Matthias, Finsterer, Josef, Gizewski, Elke R, Löscher, Wolfgang N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
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.
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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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