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Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome
Phakomatoses are a group of neurocutaneous disorders whose origin is derived from the embryonic ectoderm. These disorders affect the central nervous system, the eyes, and the skin. This article presents phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome. Moyamoya...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874860/ https://www.ncbi.nlm.nih.gov/pubmed/33603598 http://dx.doi.org/10.5114/ada.2020.102092 |
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author | Tomaszewska, Maja Strzelczuk-Judka, Lidia Ostalska-Nowicka, Danuta Jończyk-Potoczna, Katarzyna |
author_facet | Tomaszewska, Maja Strzelczuk-Judka, Lidia Ostalska-Nowicka, Danuta Jończyk-Potoczna, Katarzyna |
author_sort | Tomaszewska, Maja |
collection | PubMed |
description | Phakomatoses are a group of neurocutaneous disorders whose origin is derived from the embryonic ectoderm. These disorders affect the central nervous system, the eyes, and the skin. This article presents phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome. Moyamoya disease is a progressive and occlusive disorder of the cerebral vasculature often presenting with particular phakomatoses. This article aims to reveal why patients with phakomatoses qualify for detailed neuroimaging. |
format | Online Article Text |
id | pubmed-7874860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-78748602021-02-17 Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome Tomaszewska, Maja Strzelczuk-Judka, Lidia Ostalska-Nowicka, Danuta Jończyk-Potoczna, Katarzyna Postepy Dermatol Alergol Review Paper Phakomatoses are a group of neurocutaneous disorders whose origin is derived from the embryonic ectoderm. These disorders affect the central nervous system, the eyes, and the skin. This article presents phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome. Moyamoya disease is a progressive and occlusive disorder of the cerebral vasculature often presenting with particular phakomatoses. This article aims to reveal why patients with phakomatoses qualify for detailed neuroimaging. Termedia Publishing House 2021-01-06 2020-12 /pmc/articles/PMC7874860/ /pubmed/33603598 http://dx.doi.org/10.5114/ada.2020.102092 Text en Copyright: © 2021 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Review Paper Tomaszewska, Maja Strzelczuk-Judka, Lidia Ostalska-Nowicka, Danuta Jończyk-Potoczna, Katarzyna Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome |
title | Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome |
title_full | Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome |
title_fullStr | Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome |
title_full_unstemmed | Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome |
title_short | Phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome |
title_sort | phakomatoses and cutaneous manifestations associated with moyamoya disease and syndrome |
topic | Review Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7874860/ https://www.ncbi.nlm.nih.gov/pubmed/33603598 http://dx.doi.org/10.5114/ada.2020.102092 |
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