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
PubMed
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.