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Parkes Weber syndrome

Cutaneous flush with underlying multiple micro arteriovenous fistulas, soft tissue and skeletal hypertrophy of the affected limb
Networked: 57 relevant articles (0 outcomes, 3 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Mulliken, John B: 5 articles (09/2013 - 12/2003)
2. Burrows, Patricia E: 3 articles (05/2013 - 12/2003)
3. Boon, Laurence M: 3 articles (11/2009 - 12/2003)
4. Vikkula, Miikka: 3 articles (11/2009 - 12/2003)
5. Fishman, Steven J: 2 articles (09/2013 - 04/2011)
6. Alomari, Ahmad I: 2 articles (09/2013 - 04/2011)
7. Martínez-Cuesta, Antonio: 2 articles (11/2011 - 11/2011)
8. Redondo, Pedro: 2 articles (11/2011 - 11/2011)
9. Aguado, Leyre: 2 articles (11/2011 - 11/2011)
10. Cohen, M Michael: 2 articles (01/2010 - 10/2006)

Related Diseases

1. Hypertrophy
2. Klippel-Trenaunay-Weber Syndrome (Syndrome, Klippel-Trenaunay-Weber)
3. Arteriovenous Fistula
4. Vascular Malformations
02/01/2015 - "This case report describes propranolol treatment of vascular malformations such as Klippel-Trénaunay syndrome or Parkes-Weber syndrome in adults. "
01/01/2015 - "The Parkes Weber syndrome is a congenital vascular malformation, characterized by varicose veins, arterio-venous fistulas and overgrown limbs. "
01/01/2004 - "Within the final group are included some with a low flow, such as the Klippel-Trenaunay syndrome (venous and lymphatic venular vascular malformation associated with the muscular-skeletal hypertrophy of an extremity), and others with a high flow, such as the Parkes-Weber syndrome."
11/01/2004 - "The fast-flow vascular malformations together with arteriovenous fistulae are part of Parkes Weber syndrome, characterized by congenital red cutaneous staining, hypertrophy in girth and increasing of limb length, lymphedema, increasing skin alterations due to a distal vascular steal, and pain, all of which develop during childhood. "
04/01/2011 - "Forty-six children (27.1 percent) had another disorder: microcystic/macrocystic lymphatic malformation (19.6 percent), noneponymous combined vascular malformation (13.0 percent), capillary malformation (10.9 percent), Klippel-Trenaunay syndrome (10.9 percent), hemihypertrophy (8.7 percent), posttraumatic swelling (8.7 percent), Parkes Weber syndrome (6.5 percent), lipedema (6.5 percent), venous malformation (4.3 percent), rheumatologic disorder (4.3 percent), infantile hemangioma (2.2 percent), kaposiform hemangioendothelioma (2.2 percent), or lipofibromatosis (2.2 percent). "
5. Hemangioma (Angioma)
01/01/2015 - "All demonstrated multiple CMs, two had Parkes Weber syndrome, and two had multiple infantile hemangiomas. "
05/01/2006 - "In each generation of this family, we noted the presence of hemangiomas or capillary malformations with aggravation in the third generation and onset of Parkes-Weber syndrome. "
07/01/2007 - "The reticular variant of infantile hemangioma can be confused with other vascular anomalies in the limb, such as capillary malformation, cutis marmorata telangiectasia congenita, diffuse arteriovenous malformation (Parkes Weber syndrome) and capillary-lymphatico-venous malformation (Klippel-Trenaunay syndrome). "
04/01/2011 - "Forty-six children (27.1 percent) had another disorder: microcystic/macrocystic lymphatic malformation (19.6 percent), noneponymous combined vascular malformation (13.0 percent), capillary malformation (10.9 percent), Klippel-Trenaunay syndrome (10.9 percent), hemihypertrophy (8.7 percent), posttraumatic swelling (8.7 percent), Parkes Weber syndrome (6.5 percent), lipedema (6.5 percent), venous malformation (4.3 percent), rheumatologic disorder (4.3 percent), infantile hemangioma (2.2 percent), kaposiform hemangioendothelioma (2.2 percent), or lipofibromatosis (2.2 percent). "
07/01/2015 - "We present a case-based pictorial essay to illustrate the prenatal imaging characteristics in 11 pregnancies with vascular malformations (5 lymphatic malformations, 2 Klippel-Trenaunay syndrome, 1 venous-lymphatic malformation, 1 Parkes-Weber syndrome) and vascular tumors (1 congenital hemangioma, 1 kaposiform hemangioendothelioma). "

Related Drugs and Biologics

1. TIE Receptors (TIE Receptor Tyrosine Kinases)
2. Angiopoietins
3. Vascular Endothelial Growth Factors
4. Vascular Endothelial Growth Factor Receptors (VEGF Receptors)
5. Cutis marmorata telangiectatica congenita
6. Kaposiform Hemangioendothelioma
7. Propranolol (Inderal)
8. Dacarbazine (DIC)
9. glucuronyl glucosamine glycan sulfate (Vessel)

Related Therapies and Procedures

1. General Anesthesia