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Pediatr Dermatol ; 36(4): 524-527, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31134637

ABSTRACT

Sturge-Weber syndrome (SWS) is characterized by facial capillary malformation, leptomeningeal capillary malformations, and choroidal and episcleral vascular malformations. These malformations produce neurologic and ophthalmological symptoms including seizures and glaucoma. A premature male newborn without prenatal diagnosis presented with severe bilateral SWS and was started on systemic sirolimus and aspirin. The patient has remained seizure-free for 23 months and demonstrated an excellent response to pulsed dye laser treatment.


Subject(s)
Aspirin/therapeutic use , Infant, Premature , Seizures/prevention & control , Sirolimus/therapeutic use , Sturge-Weber Syndrome/diagnosis , Sturge-Weber Syndrome/drug therapy , Administration, Oral , Drug Therapy, Combination , Electroencephalography/methods , Humans , Infant, Newborn , Lasers, Dye/therapeutic use , Magnetic Resonance Imaging/methods , Male , Port-Wine Stain/diagnosis , Port-Wine Stain/surgery , Primary Prevention/methods , Prognosis , Risk Assessment , Severity of Illness Index , Sturge-Weber Syndrome/diagnostic imaging , Treatment Outcome
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