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Journal Article
by Zheng, Y and Peng, YM and Zhang, SJ and Li, LP and Peng, Y and Yin, Q
FRONTIERS IN GENETICS, ISSN 1664-8021, 11/2019, Volume 10
.... Alagille syndrome is an autosomal dominant multisystem disorder, usually involving hepatic, cardiac, ophthalmic, skeletal, or renal dysplasia... 
PARKES-WEBER-SYNDROME | DIAGNOSIS | Alagille syndrome | liver | vascular malformation | HUMAN JAGGED1 | COLLEGE | GENETICS & HEREDITY | Abernethy malformation | congenital heart disease | DISORDER | MUTATIONS | double gene variations | port-wine stain
Journal Article
Indian Journal of Paediatric Dermatology, ISSN 2319-7250, 10/2018, Volume 19, Issue 4, pp. 363 - 365
Klippel-Trenaunay syndrome (KTS) is characterized by the triad of varicosity of cutaneous veins, port wine stains, and soft tissue/bone overgrowth... 
Case studies | Complications and side effects | Angiomatosis | Klippel–Trenaunay syndrome | Parkes Weber syndrome | port wine stain | varicose veins | soft-tissue overgrowth
Journal Article
JAAD Case Reports, ISSN 2352-5126, 06/2019, Volume 5, Issue 6, pp. 560 - 562
Journal Article
Italian Journal of Anatomy and Embryology, ISSN 1122-6714, 2017, Volume 122, Issue 3, pp. 155 - 156
...Key words History of medicine, Klippel-Trénaunay-Weber syndrome, Madonna of the Rocks, Parkes Weber syndrome. Sir: Leonardo da Vinci is considered amongst... 
Madonna of the Rocks | History of medicine | Klippel-Trénaunay-Weber syndrome | Parkes Weber syndrome
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 10/2006, Volume 140A, Issue 19, pp. 2013 - 2038
...; Kasabach‐Merritt phenomenon; Sturge‐Weber syndrome, Klippel‐Trenaunay syndrome, and Parkes Weber syndrome... 
VEGFRs | FOXC2 | vasculogenesis | ECM1 | angiopoietins | EFNB2 | tufted angioma | Glomulin (GLMN) | SOX18 | FGFs/FGFRs | Parkes Weber syndrome | lymphatic malformation | noninvoluting congenital hemangioma (NICH) | EPHB4 | GLUT1 | EGFL7 | TIEs | angiogenesis | rapidly involuting congenital hemangioma (RICH) | neovascularization | Kasabach‐Merritt phenomenon | anti‐angiogenic therapy | Kaposiform hemangioendothelioma | Klippel‐Trenaunay syndrome | FL4 | retinoic acid | infantile hemangioma | RASA1 | VEGFs | neuropilin 1 (NRP1) | hematopoietic stem cells | Sturge‐Weber syndrome | Kaposi-form hemangioendothelioma | Kasabach-Merritt phenomenon | Angiogenesis | Rapidly involuting congenital hemangioma (RICH) | Noninvoluting congenital hemangioma (NICH) | Lymphatic malformation | Tufted angioma | Infantile hemangioma | Vasculogenesis | INTRAOSSEOUS HEMANGIOMAS | MARMORATA TELANGIECTATICA CONGENITA | VENOUS MALFORMATIONS | KLIPPEL-TRENAUNAY-SYNDROME | ENDOTHELIAL-CELLS | GENETICS & HEREDITY | CUTIS MARMORATA | Klippel-Trenaunay syndrome | anti-angiogenic therapy | WEBER-SYNDROME | SPINDLE-CELL HEMANGIOENDOTHELIOMA | GROWTH-FACTOR RECEPTORS | Sturge-Weber syndrome | Gloniulin (GLMN) | TRANSCRIPTION FACTOR | Receptors, Vascular Endothelial Growth Factor - physiology | Blood Vessels - growth & development | Blood Vessels - abnormalities | Humans | Neoplasms, Vascular Tissue - etiology | Neovascularization, Pathologic | Lymphatic Vessels - abnormalities | Male | Neoplasms, Vascular Tissue - congenital | Syndrome | Morphogenesis | Angiogenesis Inhibitors - therapeutic use | Female | Blood Vessels - physiology | Child | Neoplasms, Vascular Tissue - drug therapy | Vascular Endothelial Growth Factor A - physiology | Neovascularization, Physiologic
Journal Article
Indian Journal of Dermatology, ISSN 0019-5154, 2014, Volume 59, Issue 4, pp. 406 - 408
.... Parkes-Weber syndrome is a triad of arterio-venous malformation with varicose veins with bony and soft-tissue hypertrophy involving the extremity... 
Parkes-Weber syndrome | Stewart-Bluefarb syndrome | Stewart-Bluefarb acroangiodermatitis | DERMATOLOGY | Case studies | Reports | Angiomatosis | Acrodermatitis | Diagnosis | Case Report
Journal Article
Journal of Ultrasound in Medicine, ISSN 0278-4297, 09/2016, Volume 35, Issue 9, pp. 2057 - 2065
Klippel‐Trénaunay syndrome (KTS) is a rare congenital malformation characterized by a triad of clinical presentations: (1... 
angio‐osteohypertrophy syndrome | Klippel‐Trénaunay syndrome | vascular ultrasound | Parkes‐Weber syndrome | sonography | venous malformations
Journal Article
Human mutation, ISSN 1059-7794, 2008, Volume 29, Issue 7, pp. 959 - 965
Journal Article
Jornal vascular brasileiro, ISSN 1677-5449, 11/2017, Volume 16, Issue 4, pp. 320 - 324
Abstract Parkes-Weber syndrome is a congenital vascular disease that comprises capillary, venous, lymphatic, and arteriovenous malformations... 
nevus | arteriovenous malformations | angiodisplasias | síndrome de Klippel-Trenaunay | Klippel-Trenaunay syndrome | síndrome de Parkes-Weber | Parkes-Weber syndrome | angiodysplasia | malformações arteriovenosas | Case Report
Journal Article
Indian Journal of Surgery, ISSN 0972-2068, 4/2015, Volume 77, Issue S1, pp. 130 - 134
.... Patients with Parkes Weber syndrome have clinically significant micro- or macrofistulous arteriovenous shunts, affecting usually one extremity... 
Vascular malformations | Plastic Surgery | Massive arteriolisation | Cardiomegaly | Medicine & Public Health | Cardiac Surgery | Surgery | Arteriovenous shunts | Neurosurgery | Thoracic Surgery | Parkes Weber syndrome | Pediatric Surgery | SURGERY | Legs | Congenital diseases | Veins & arteries | Case Report
Journal Article