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An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks

Moyamoya disease is a rare, chronic, idiopathic progressive disease characterized by irreversible vascular occlusion of the vessels of the Circle of Willis. The disease was initially considered to be limited to the East Asian population, but now the disease is being reported all over the globe in pe...

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Autores principales: Sapra, Amit, Bhandari, Priyanka, Dix, Rebecca, Sharma, Shivani, Ranjit, Eukesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489789/
https://www.ncbi.nlm.nih.gov/pubmed/32944454
http://dx.doi.org/10.7759/cureus.9736
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author Sapra, Amit
Bhandari, Priyanka
Dix, Rebecca
Sharma, Shivani
Ranjit, Eukesh
author_facet Sapra, Amit
Bhandari, Priyanka
Dix, Rebecca
Sharma, Shivani
Ranjit, Eukesh
author_sort Sapra, Amit
collection PubMed
description Moyamoya disease is a rare, chronic, idiopathic progressive disease characterized by irreversible vascular occlusion of the vessels of the Circle of Willis. The disease was initially considered to be limited to the East Asian population, but now the disease is being reported all over the globe in people of multiple ethnicities. It is crucial that clinicians are aware of the disease and its presentation to prevent under-recognition of the condition. We describe the case of a 44-year-old Caucasian female with a history of hypertension, depression, gastroesophageal reflux disease (GERD), and morbid obesity diagnosed with Moyamoya disease after she presented to the emergency department with recurrent stroke-like symptoms.
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spelling pubmed-74897892020-09-16 An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks Sapra, Amit Bhandari, Priyanka Dix, Rebecca Sharma, Shivani Ranjit, Eukesh Cureus Family/General Practice Moyamoya disease is a rare, chronic, idiopathic progressive disease characterized by irreversible vascular occlusion of the vessels of the Circle of Willis. The disease was initially considered to be limited to the East Asian population, but now the disease is being reported all over the globe in people of multiple ethnicities. It is crucial that clinicians are aware of the disease and its presentation to prevent under-recognition of the condition. We describe the case of a 44-year-old Caucasian female with a history of hypertension, depression, gastroesophageal reflux disease (GERD), and morbid obesity diagnosed with Moyamoya disease after she presented to the emergency department with recurrent stroke-like symptoms. Cureus 2020-08-14 /pmc/articles/PMC7489789/ /pubmed/32944454 http://dx.doi.org/10.7759/cureus.9736 Text en Copyright © 2020, Sapra et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Family/General Practice
Sapra, Amit
Bhandari, Priyanka
Dix, Rebecca
Sharma, Shivani
Ranjit, Eukesh
An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks
title An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks
title_full An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks
title_fullStr An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks
title_full_unstemmed An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks
title_short An Interesting Case of Moyamoya Disease, a Rare Cause of Transient Ischemic Attacks
title_sort interesting case of moyamoya disease, a rare cause of transient ischemic attacks
topic Family/General Practice
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489789/
https://www.ncbi.nlm.nih.gov/pubmed/32944454
http://dx.doi.org/10.7759/cureus.9736
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