Brain small vessel disease 2A, autosomal dominant

Any porencephaly in which the cause of the disease is a mutation in the COL4A2 gene.

Also known as: COL4A2 porencephaly, brain small vessel disease 2, porencephaly 2, porencephaly type 2, POREN2

11 clinical trials for this condition and its sub-types, 1 tagged with Brain small vessel disease 2A, autosomal dominant itself.