From recent studies, COL4A1 ", suggesting genetic predisposition within the family, that encodes type IV collagen ?1 chain has shown to be associated with and present in patients with porencephaly . " COL4A1 " mutation causes a variety of phenotypes, including porencephaly, infantile hemiplegia, and cerebral small vessel diseases involving both stroke and infarction.
22.
From recent studies, COL4A1 ", suggesting genetic predisposition within the family, that encodes type IV collagen ?1 chain has shown to be associated with and present in patients with porencephaly . " COL4A1 " mutation causes a variety of phenotypes, including porencephaly, infantile hemiplegia, and cerebral small vessel diseases involving both stroke and infarction.
