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Down Syndrome with Moyamoya Disease: A Case Series
Down syndrome (DS), resulting from trisomy 21, is a common cause of mental retardation. Around 20,000 babies with DS are born every year in India. There is an increased risk of cerebral infarction in children with DS, the common causes being thromboembolism secondary to atrioventricular canal defect...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057204/ https://www.ncbi.nlm.nih.gov/pubmed/30090136 http://dx.doi.org/10.4103/jpn.JPN_116_17 |
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author | Kumar, Pawan Panigrahi, Inusha Sankhyan, Naveen Ahuja, Chirag Goyadi, Prasoon K. |
author_facet | Kumar, Pawan Panigrahi, Inusha Sankhyan, Naveen Ahuja, Chirag Goyadi, Prasoon K. |
author_sort | Kumar, Pawan |
collection | PubMed |
description | Down syndrome (DS), resulting from trisomy 21, is a common cause of mental retardation. Around 20,000 babies with DS are born every year in India. There is an increased risk of cerebral infarction in children with DS, the common causes being thromboembolism secondary to atrioventricular canal defects, right-to-left shunting, myocardial dysmotility, or cardiac valvular abnormalities. Stroke due to other causes can also occur in patients with DS, and one of these is moyamoya disease. This can be diagnosed by magnetic resonance imaging and/or angiography in these patients. Here we report four cases of moyamoya disease in young patients with DS aged 2–3½ years, of a total of 500 cases with DS registered in the Genetic Clinic. |
format | Online Article Text |
id | pubmed-6057204 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60572042018-08-08 Down Syndrome with Moyamoya Disease: A Case Series Kumar, Pawan Panigrahi, Inusha Sankhyan, Naveen Ahuja, Chirag Goyadi, Prasoon K. J Pediatr Neurosci Case Report Down syndrome (DS), resulting from trisomy 21, is a common cause of mental retardation. Around 20,000 babies with DS are born every year in India. There is an increased risk of cerebral infarction in children with DS, the common causes being thromboembolism secondary to atrioventricular canal defects, right-to-left shunting, myocardial dysmotility, or cardiac valvular abnormalities. Stroke due to other causes can also occur in patients with DS, and one of these is moyamoya disease. This can be diagnosed by magnetic resonance imaging and/or angiography in these patients. Here we report four cases of moyamoya disease in young patients with DS aged 2–3½ years, of a total of 500 cases with DS registered in the Genetic Clinic. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6057204/ /pubmed/30090136 http://dx.doi.org/10.4103/jpn.JPN_116_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 Kumar, Pawan Panigrahi, Inusha Sankhyan, Naveen Ahuja, Chirag Goyadi, Prasoon K. Down Syndrome with Moyamoya Disease: A Case Series |
title | Down Syndrome with Moyamoya Disease: A Case Series |
title_full | Down Syndrome with Moyamoya Disease: A Case Series |
title_fullStr | Down Syndrome with Moyamoya Disease: A Case Series |
title_full_unstemmed | Down Syndrome with Moyamoya Disease: A Case Series |
title_short | Down Syndrome with Moyamoya Disease: A Case Series |
title_sort | down syndrome with moyamoya disease: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057204/ https://www.ncbi.nlm.nih.gov/pubmed/30090136 http://dx.doi.org/10.4103/jpn.JPN_116_17 |
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