Phakomatosis pigmentovascularis with Sturge-Weber syndrome: a case report

G Uysal; A Güven; B Ozhan; M H Oztürk; A H Mutluay; O Tulunay

doi:10.1111/j.1346-8138.2000.tb02208.x

Phakomatosis pigmentovascularis with Sturge-Weber syndrome: a case report

J Dermatol. 2000 Jul;27(7):467-70. doi: 10.1111/j.1346-8138.2000.tb02208.x.

Authors

G Uysal¹, A Güven, B Ozhan, M H Oztürk, A H Mutluay, O Tulunay

Affiliation

¹ Department of Pediatric Infectious Disease, Social Security Institution Children's Hospital, Ankara, Turkey.

PMID: 10935346
DOI: 10.1111/j.1346-8138.2000.tb02208.x

Abstract

We describe here a Turkish girl with pigmentovascularis type 2b, consisting of disseminated Mongolian-spot-like maculae and unilateral Sturge-Weber angiomatosis.

Publication types

Case Reports

MeSH terms

Anticonvulsants / administration & dosage
Biopsy, Needle
Brain / pathology
Female
Follow-Up Studies
Humans
Infant
Magnetic Resonance Imaging
Port-Wine Stain / diagnosis
Port-Wine Stain / pathology*
Seizures / diagnosis
Seizures / drug therapy
Sturge-Weber Syndrome / diagnosis
Sturge-Weber Syndrome / drug therapy
Sturge-Weber Syndrome / pathology*

Substances

Anticonvulsants