Fowler vasculopathy

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Fowler vasculopathy

ORPHA:221126Malformation syndrome

Also called Cerebral proliferative glomeruloid vasculopathy · Encephaloclastic proliferative vasculopathy · Hydrocephaly/hydranencephaly due to cerebral vasculopathy · Proliferative vasculopathy and hydranencephaly/hydrocephaly

What it is

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.

Key facts

Prevalence
<1 / 1 000 000
Age of onset
Antenatal, Neonatal
Inheritance
Autosomal recessive
Classified as
Malformation syndrome

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Gene

FLVCR2Disease-causing germline mutation(s)

ICD-10 codes

Q04.8filed under a broader ICD-10 category — shared with 40 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

OMIM 225790UMLS C1856972

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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