Parkes-Weber syndrome

Parkes-Weber syndrome

(1) Klippel-Trenaunay syndrome, see there.
(2) Sturge-Weber syndrome, see there.
References in periodicals archive ?
The differential diagnosis includes Parkes-Weber syndrome, neurofibromatosis, lymphedema, and CLOVES syndrome.
This entity should be distinguished from Parkes-Weber syndrome, which is similar, but features formation of arteriovenous malformations (leading to high output cardiac failure) and no lymphatic malformations.
The ISSVA classification is useful for identifying clinical landmarks, because some of the entities are associated with skin lesions, as is the case for hereditary hemorrhagic telangiectasia, Klippel-Trenaunay-Weber syndrome, Parkes-Weber syndrome, while other entities do not include lesions of the skin, for example angiodysplasia and arteriovenous malformations (Lowe et al 2012).