| Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. | |
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MedLine Citation:
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PMID: 15575847 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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We describe a 23-month-old child with phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. Phakomatosis pigmentovascularis type IIb is a rare cutaneous malformation characterized by the simultaneous occurrence of nevus flammeus and melanocytic nevi. A brief review of the literature is presented and classification of this rare disease is discussed. |
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Authors:
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Ahmad Al Robaee; Nusrat Banka; Abdullah Alfadley |
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Publication Detail:
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Type: Case Reports; Journal Article; Review |
Journal Detail:
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Title: Pediatric dermatology Volume: 21 ISSN: 0736-8046 ISO Abbreviation: Pediatr Dermatol Publication Date: 2004 Nov-Dec |
Date Detail:
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Created Date: 2004-12-03 Completed Date: 2005-06-28 Revised Date: 2009-03-03 |
Medline Journal Info:
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Nlm Unique ID: 8406799 Medline TA: Pediatr Dermatol Country: United States |
Other Details:
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Languages: eng Pagination: 642-5 Citation Subset: IM |
Affiliation:
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Department of Medicine, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Brain
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pathology Electroencephalography Female Humans Infant Magnetic Resonance Imaging Neurocutaneous Syndromes / classification, complications*, diagnosis Port-Wine Stain / diagnosis, etiology Seizures / etiology Skin / pathology* Sturge-Weber Syndrome / complications* |
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