Document Detail

Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome.
MedLine Citation:
PMID:  20609155     Owner:  NLM     Status:  MEDLINE    
We present two rare cases of phacomatosis pigmentovascularis type IIb, with one patient demonstrating concurrent Sturge-Weber syndrome and Klippel-Trenaunay syndrome. To the best of our knowledge, this is the second infantile case meeting diagnostic criteria for systemic phacomatosis pigmentovascularis type IIb, Sturge-Weber syndrome and Klippel-Trenaunay syndrome in the English language literature.
Lindsey B Finklea; Melinda R Mohr; Molly M Warthan; David H Darrow; Judith V Williams
Related Documents :
16225815 - Comorbidity of epilepsy and headache in patients with sturge-weber syndrome.
20451865 - Persistent fetal vasculature and spontaneous hyphema in a patient with klippel-trénaun...
6619945 - Congenital neural abnormalities presenting with mirror movements in a patient with klip...
15105685 - Klippel-feil syndrome presenting with bilateral thoracic outlet syndrome.
3287365 - Prenatal ultrasound diagnosis of the holt-oram syndrome.
6486165 - Gross anatomical studies of a newborn infant with the meckel syndrome.
Publication Detail:
Type:  Case Reports; Journal Article; Review    
Journal Detail:
Title:  Pediatric dermatology     Volume:  27     ISSN:  1525-1470     ISO Abbreviation:  Pediatr Dermatol     Publication Date:    2010 May-Jun
Date Detail:
Created Date:  2010-07-08     Completed Date:  2010-10-25     Revised Date:  2011-01-11    
Medline Journal Info:
Nlm Unique ID:  8406799     Medline TA:  Pediatr Dermatol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  303-5     Citation Subset:  IM    
Department of Dermatology, Eastern Virginia Medical School, Norfolk, Virginia 23507, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Infant, Newborn
Klippel-Trenaunay-Weber Syndrome / diagnosis*
Neurocutaneous Syndromes / diagnosis*
Sturge-Weber Syndrome / diagnosis*
Vascular Malformations / diagnosis*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Penile erosions associated with foscarnet therapy in a child.
Next Document:  Dermal melanocytosis of the helix.