Severe Hemophilia A and Moyamoya Syndrome in a 19-Year-Old Boy Caused by Xq28 Microdeletion

Severe hemophilia A and moyamoya (SHAM) syndrome is a rare condition that combines hemophilia A and moyamoya disease (MMD) due to an Xq28 microdeletion encompassing the F8 and BRCC3 genes. Here, we report the case of a 19-year-old male patient with hemophilia A and hypogonadism that presented with r...

Olles dieđut

Bibliográfalaš dieđut

Váldodahkkit:	Evangelia Tzeravini, Stamatia Samara, Anna Kouramba, Georgios Vakrinos, Athina Efthimiou, Maria Tzetis, Theodoros Androutsakos
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	Karger Publishers 2022-05-01
Ráidu:	Case Reports in Neurology
Fáttát:	hemophilia a moyamoya syndrome stroke sham syndrome
Liŋkkat:	https://www.karger.com/Article/FullText/524482
Fáddágilkorat:	Lasit fáddágilkoriid Eai fáddágilkorat, Lasit vuosttaš fáddágilkora!