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Pediatric Moyamoya disease
BACKGROUND: Moyamoya disease (MMD) is a progressive cerebrovascular occlusive disease of the bilateral internal carotid arteries that leads to a compensatory abnormal vascular network at the base of the brain. Its average annual incidence 0.54 per 100,000 population but it is the most common pediatr...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700478/ https://www.ncbi.nlm.nih.gov/pubmed/23826451 http://dx.doi.org/10.12659/AJCR.889170 |
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author | Nagiub, Mohamed Allarakhia, Iqbal |
author_facet | Nagiub, Mohamed Allarakhia, Iqbal |
author_sort | Nagiub, Mohamed |
collection | PubMed |
description | BACKGROUND: Moyamoya disease (MMD) is a progressive cerebrovascular occlusive disease of the bilateral internal carotid arteries that leads to a compensatory abnormal vascular network at the base of the brain. Its average annual incidence 0.54 per 100,000 population but it is the most common pediatric cerebrovascular disease in East Asia. The reported incidence in USA is approximately 0.086 per 100,000 patients. CASE REPORT: We present a case of Moyamoya disease that was to detected in a 7-year-old female who presented with transient altered mental status. CONCLUSIONS: Moyamoya disease can be diagnosed if history, physical exam and brain imaging is highly suspicious. Conventional angiography remains the gold standard for diagnosis and aids in surgical planning for patients with suspected Moyamoya disease. |
format | Online Article Text |
id | pubmed-3700478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37004782013-07-03 Pediatric Moyamoya disease Nagiub, Mohamed Allarakhia, Iqbal Am J Case Rep Case Report BACKGROUND: Moyamoya disease (MMD) is a progressive cerebrovascular occlusive disease of the bilateral internal carotid arteries that leads to a compensatory abnormal vascular network at the base of the brain. Its average annual incidence 0.54 per 100,000 population but it is the most common pediatric cerebrovascular disease in East Asia. The reported incidence in USA is approximately 0.086 per 100,000 patients. CASE REPORT: We present a case of Moyamoya disease that was to detected in a 7-year-old female who presented with transient altered mental status. CONCLUSIONS: Moyamoya disease can be diagnosed if history, physical exam and brain imaging is highly suspicious. Conventional angiography remains the gold standard for diagnosis and aids in surgical planning for patients with suspected Moyamoya disease. International Scientific Literature, Inc. 2013-05-03 /pmc/articles/PMC3700478/ /pubmed/23826451 http://dx.doi.org/10.12659/AJCR.889170 Text en © Am J Case Rep, 2013 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License |
spellingShingle | Case Report Nagiub, Mohamed Allarakhia, Iqbal Pediatric Moyamoya disease |
title | Pediatric Moyamoya disease |
title_full | Pediatric Moyamoya disease |
title_fullStr | Pediatric Moyamoya disease |
title_full_unstemmed | Pediatric Moyamoya disease |
title_short | Pediatric Moyamoya disease |
title_sort | pediatric moyamoya disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700478/ https://www.ncbi.nlm.nih.gov/pubmed/23826451 http://dx.doi.org/10.12659/AJCR.889170 |
work_keys_str_mv | AT nagiubmohamed pediatricmoyamoyadisease AT allarakhiaiqbal pediatricmoyamoyadisease |