Genetic stroke syndromes

Autosomal dominant-- CADASIL, VHL, cavernous malformations (CCM1), most types of amyloidosis, Hereditary hemorrhagic telangiectasia, and PCK disease.

Autosomal recessive-- virtually all clotting disorders (pro C res due to Leiden FV mutation, PT 20210, pro C, pro S, VWF def, AT 3, plasminogen def, Marfan, Fabry, SCD, heparin cof 2, F XII, hyper homocyst, hyper cysteinemia,


Maternal-- MELAS