Moyamoya Syndrome in a 32-Year-Old Male With Sickle Cell Anemia

被引：6

作者：

Yamani, Mariam ^{[1
]}

Obaid, Elaf F. ^{[2
]}

Hemida, Amr H. ^{[2
]}

机构：

[1] Umm Al Qura Univ, Med, Mecca, Saudi Arabia

[2] Al Noor Specialist Hosp, Internal Med, Mecca, Saudi Arabia

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2020年 / 12卷 / 08期

关键词：

moyamoya disease; moyamoya syndrome; sickle cell disease; vasculopathy;

D O I：

10.7759/cureus.10001

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Moyamoya disease (MMD) is an unusual vasculopathy in which the blood vessels of the brain are occluded, resulting in thrombosis. When MMD occurs in association with an underlying pathology, it is known as moyamoya syndrome. The association of moyamoya syndrome with sickle cell disease is uncommon. Herein, we report a case of moyamoya syndrome in a 32-year-old male adult patient.

引用

页数：5

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