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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...

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Autores principales: Nagiub, Mohamed, Allarakhia, Iqbal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2013
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.
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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
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