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Parkes Weber syndrome
rareA rare congenital complex vascular malformation syndrome characterized by overgrowth of a limb (most commonly a leg) involving bones and soft tissue, in association with capillary malformations usually in the form of port-wine stains and multiple arteriovenous fistulas with high-flow arteriovenous shunting. The latter can also lead to other severe complications including abnormal bleeding and heart failure. Lymphatic malformations may also be present.
- Identifiers
- MONDO:0700325 Orphanet:90307
- Part of
- Congenital vascular malformation
- Also known as
- PWS
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