患有Fanconi贫血的儿童患有莫亚莫亚病:异常或并发症
Samin Alavi1, Mitra Khalili2, Zahra Khaffafpour3
1Hematology/Oncology, Pediatric Congenital Hematologic Disorders Research Center, Research Institute for Children's Health, Shahid Beheshti University of Medical Sciences, Tehran, IRN.
Cureus
|March 21, 2024
概括
芬科尼贫血 (FA) 是一种罕见的遗传性疾病,可以表现为神经复杂症,如莫亚莫亚病 (MMD). 这个案例突出了一个患有FA的年轻男孩,他患有MMD,这引发了有关FA的原因的问题.
科学领域:
- 神经学 神经学
- 血液学 血液学 血液学
- 遗传学 是一个遗传学.
背景情况:
- 芬科尼贫血 (FA) 是一种遗传性骨髓衰竭综合征.
- FA的特点是先天性异常和癌症风险增加.
- 神经学并发症是公认的,但在FA中不太常见.
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