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Parkes Weber syndrome
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Parkes Weber syndrome : ウィキペディア英語版
Parkes Weber syndrome

Parkes Weber Syndrome (PWS) is an uncommon congenital vascular malformation (CVM) similar to Klippel–Trénaunay syndrome, but has its own distinct conditions. It was first described in 1907 by British dermatologist Frederick Parkes Weber.〔 It is only found in about 0.3% of the world population.〔
== Characteristics ==
PWS is characterized by the venous malformations, cutaneous capillary malformations, and lymphatic malformations found in Klippel–Trénaunay–Weber syndrome along with arteriovenous malformation.〔 It also can include fistulas occurring with skeletal or soft tissue hypertrophy.〔 The syndrome can affect multiple limbs, the trunk, and the head. The body’s lower extremities are most commonly affected.〔

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