Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare, genetic neurological disorder characterized by hydranencephaly, distinctive glomeruloid vasculopathy in the central nervous system and retina, polyhydramnios and fetal akinesia with arthrogryposis. The disorder is usually prenatally lethal. In rare reported cases that survived beyond infancy, severe intellectual and neurologic disability with seizures, microcephaly and absence of functional movements were reported. Disease data Classification Malformation syndrome Synonyms Cerebral proliferative glomeruloid vasculopathy Encefaloklastyczna waskulopatia proliferacyjna Proliferacyjna waskulopatia kłębuszkowa mózgu Waskulopatia proliferacyjna i hydrocefalia/hydranencefalia Wodogłowie/hydranencefalia z powodu waskulopatii mózgowej Encephaloclastic proliferative vasculopathy Hydrocephaly/hydranencephaly due to cerebral vasculopathy Proliferative vasculopathy and hydranencephaly/hydrocephaly ORPHA code 221126 OMIM code 225790 ICD10 code Q04.8 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl