Clinical spectrum of capillary malformation-arteriovenous malformation syndrome presenting to a pediatric dermatology practice: A retrospective study

Pediatric Dermatology

Volumn 32, Issue 1, 2015, Pages 76-84

  Weitz, Nicole A ^a   Lauren, Christine T ^b   Behr, Gerald G ^b   Wu, June K ^b   Kandel, Jessica J ^c   Meyers, Philip M ^b   Sultan, Sally ^b   Anyane Yeboa, Kwame ^b   Morel, Kimberly D ^b   Garzon, Maria C ^b  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b Department of Dermatology College of Phys and Surg Columbia University ^*  (United States)

^c UNIVERSITY OF CHICAGO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOOSTEOHYPERTROPHY SYNDROME; ARTERIOVENOUS MALFORMATION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CAPILLARY HEMANGIOMA; CAPILLARY MALFORMATION ARTERIOVENOUS MALFORMATION SYNDROME; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONSULTATION; FAMILY HISTORY; FEMALE; GENE MUTATION; HUMAN; INFANT; MALE; MUTATOR GENE; NEWBORN; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; RASA1 GENE; RETROSPECTIVE STUDY; SCHOOL CHILD; SKIN EXAMINATION; SYMPTOMATOLOGY; ARTERIOVENOUS MALFORMATIONS; CAPILLARY; CONGENITAL MALFORMATION; GENETICS; MUTATION; PORT-WINE STAIN; PRESCHOOL CHILD;

GUANOSINE TRIPHOSPHATASE ACTIVATING PROTEIN; RASA1 PROTEIN, HUMAN;

ARTERIOVENOUS MALFORMATIONS; CAPILLARIES; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; P120 GTPASE ACTIVATING PROTEIN; PORT-WINE STAIN; RETROSPECTIVE STUDIES;

EID: 84921840232     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/pde.12384     Document Type: Article

References (18)

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