Fowler vasculopathy

Orpha code: 221126OMIM code: 225790

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
-

No additional description.

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