Cortical malformations characterized by white matter-lined cleft or cyst associated with ISCHEMIA and hemorrhagic insults. Symptoms include delayed growth and development, HYPOTONIA; SEIZURES; SPASTIC HEMIPLEGIA and MACROCEPHALY; MICROCEPHALY; or HYDROCEPHALUS. Mutations in the genes encoding COLLAGEN TYPE IV are associated with familial types.
Familjär porencefali — Medfödd porencefali — Posttraumatisk porencefali
Porencephalies — Congenital Porencephaly — Porencephaly, Congenital — Developmental Porencephaly — Porencephaly, Developmental — Porencephaly, Type 1 — Type 1 Porencephaly — Porencephaly, Familial — Porencephaly, Type 1, Autosomal Dominant — Autosomal Dominant Porencephaly Type 1 — Infantile Hemiplegia with Porencephaly — Porencephaly Type 1 — Familial Porencephaly — Familial Porencephalic White Matter Disease — Retinal Arteriolar Tortuosity, Infantile Hemiparesis, and Leukoencephalopathy, Autosomal Dominant — Col4a1-Related Brain Small-Vessel Disease — Col4a1 Related Brain Small Vessel Disease — Brain Small-Vessel Disease with Hemorrhage — Brain Small Vessel Disease with Hemorrhage — Leukoencephalopathy with Axenfeld-Rieger Anomaly — Leukoencephalopathy with Axenfeld Rieger Anomaly — Brain Small Vessel Disease With Axenfeld-Rieger Anomaly — Brain Small Vessel Disease With Axenfeld Rieger Anomaly — Encephaloclastic Porencephaly — Porencephaly, Encephaloclastic — Posttraumatic Porencephaly — Porencephalies, Posttraumatic — Porencephaly, Posttraumatic — Posttraumatic Porencephalies — Post-traumatic Porencephaly — Porencephalies, Post-traumatic — Porencephaly, Post-traumatic — Post-traumatic Porencephalies — Post traumatic Porencephaly