Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report

Seckel syndrome and Moyamoya diseases are different entities that rarely associated with each other. Several cases presenting with both these diseases were reported. Intracerebral artery aneurysms and collateral vessels can be seen with Moyamoya. They are commonly treated with medical treatment. We...

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Autores principales: Gunesli, Aylin, Andic, Cagatay, Alkan, Ozlem, Erol, Ilknur, Suner, Halil Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057185/
https://www.ncbi.nlm.nih.gov/pubmed/30090148
http://dx.doi.org/10.4103/jpn.JPN_96_17
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author Gunesli, Aylin
Andic, Cagatay
Alkan, Ozlem
Erol, Ilknur
Suner, Halil Ibrahim
author_facet Gunesli, Aylin
Andic, Cagatay
Alkan, Ozlem
Erol, Ilknur
Suner, Halil Ibrahim
author_sort Gunesli, Aylin
collection PubMed
description Seckel syndrome and Moyamoya diseases are different entities that rarely associated with each other. Several cases presenting with both these diseases were reported. Intracerebral artery aneurysms and collateral vessels can be seen with Moyamoya. They are commonly treated with medical treatment. We present a 12-years old patient with both Seckel syndrome and Moyamoya disease presented with middle cerebral artery aneurysm which was treated with endovascular modalities.
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spelling pubmed-60571852018-08-08 Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report Gunesli, Aylin Andic, Cagatay Alkan, Ozlem Erol, Ilknur Suner, Halil Ibrahim J Pediatr Neurosci Case Report Seckel syndrome and Moyamoya diseases are different entities that rarely associated with each other. Several cases presenting with both these diseases were reported. Intracerebral artery aneurysms and collateral vessels can be seen with Moyamoya. They are commonly treated with medical treatment. We present a 12-years old patient with both Seckel syndrome and Moyamoya disease presented with middle cerebral artery aneurysm which was treated with endovascular modalities. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6057185/ /pubmed/30090148 http://dx.doi.org/10.4103/jpn.JPN_96_17 Text en Copyright: © 2018 Journal of Pediatric Neurosciences http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Gunesli, Aylin
Andic, Cagatay
Alkan, Ozlem
Erol, Ilknur
Suner, Halil Ibrahim
Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report
title Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report
title_full Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report
title_fullStr Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report
title_full_unstemmed Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report
title_short Endovascular Treatment of a Patient with Moyamoya Disease and Seckel Syndrome: A Case Report
title_sort endovascular treatment of a patient with moyamoya disease and seckel syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057185/
https://www.ncbi.nlm.nih.gov/pubmed/30090148
http://dx.doi.org/10.4103/jpn.JPN_96_17
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