Phakomatosis Pigmentovascularis with Sturge-Weber Syndrome: A Case Report

Author:

Uysal Gülnar1,Güven Alev2,Özhan Bayram3,Öztürk M. Halil4,Mutluay A. Hürriyet5,Tulunay Özden6

Affiliation:

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

2. Department of Pediatric Neurology; Social Security Institution Children's Hospital; Ankara Turkey

3. Social Security Institution Children's Hospital; Ankara Turkey

4. Med-Mar Medical Imaging Center; Ankara Turkey

5. Department of Ophthalmology; Social Security Institution Hospital; Ankara Turkey

6. Department of Pathology; Ankara University; Ankara Turkey

Publisher

Wiley

Subject

Dermatology,General Medicine

Reference12 articles.

1. Phacomatosis pigmentovascularis;Ota;Jpn J Dermatol,1947

2. A variant of phacomatosis pigmentovascularis;Hasegawa;Skin Res,1979

3. Phakomatosis pigmentovascularis type IV a;Hasegawa;Arch Dermatol,1985

4. Phakomatosis pigmentovascularis type IIIb associated with Moyamoya disease;Tsuruta;Pediatr Dermatol,1999

5. Phakomatosis pigmentovascularis type IIb with iris mammillations;Gilliam;Arch Dermatol,1993

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1. Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review;American Journal of Medical Genetics Part A;2019-03-28

2. Phakomatosis pigmentovascularis: Implications for severity with special reference to Mongolian spots associated with Sturge–Weber and Klippel–Trenaunay syndromes;American Journal of Medical Genetics Part A;2008

3. Phacomatosis cesioflammea with unilateral lipohypoplasia;American Journal of Medical Genetics Part A;2008

4. Klippel-Tranaunay, Parkes Weber and Sturge-Weber Syndromes (Including Kasabach-Merrit Phenomena);Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes;2008

5. Phakomatosis Pigmentovascularis;Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes;2008

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