Sturge-Weber syndrome: about a case

Sturge-Weber syndrome (SWS) or encephalofacial angiomatosis is a rare neurocutaneous and congenital ocular syndrome. It can cause two malformations: congenital facial capillary planar angioma and leptomeningal venous-capillary angioma (most often parieto-occipital homolateral angioma). Neuroimaging,...

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Published inThe Pan African medical journal Vol. 36; p. 273
Main Authors Doumiri, Meriem, Labied, Mohamed, Salam, Siham, Laoudiyi, Dalal, Chbani, Kamilia, Ouzidane, Lahcen
Format Journal Article
LanguageFrench
Published Uganda 12.08.2020
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Abstract Sturge-Weber syndrome (SWS) or encephalofacial angiomatosis is a rare neurocutaneous and congenital ocular syndrome. It can cause two malformations: congenital facial capillary planar angioma and leptomeningal venous-capillary angioma (most often parieto-occipital homolateral angioma). Neuroimaging, in particular magnetic resonance imaging (MRI), plays an important role in the diagnosis, ideally before the occurrence of neuro-ocular complications. We report the case of a child in whom SWS was suspected based on facial angioma and pharmaco-resistant epilepsy.
AbstractList Sturge-Weber syndrome (SWS) or encephalofacial angiomatosis is a rare neurocutaneous and congenital ocular syndrome. It can cause two malformations: congenital facial capillary planar angioma and leptomeningal venous-capillary angioma (most often parieto-occipital homolateral angioma). Neuroimaging, in particular magnetic resonance imaging (MRI), plays an important role in the diagnosis, ideally before the occurrence of neuro-ocular complications. We report the case of a child in whom SWS was suspected based on facial angioma and pharmaco-resistant epilepsy.
Author Doumiri, Meriem
Laoudiyi, Dalal
Chbani, Kamilia
Salam, Siham
Labied, Mohamed
Ouzidane, Lahcen
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  givenname: Lahcen
  surname: Ouzidane
  fullname: Ouzidane, Lahcen
  organization: Service de la Radiologie Pédiatrique, Hôpital Harouchi, Casablanca, Morocco
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Keywords MRI
Sturge-Weber
planar angioma
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Snippet Sturge-Weber syndrome (SWS) or encephalofacial angiomatosis is a rare neurocutaneous and congenital ocular syndrome. It can cause two malformations: congenital...
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SubjectTerms Child
Drug Resistant Epilepsy - etiology
Hemangioma - etiology
Hemangioma - pathology
Humans
Magnetic Resonance Imaging
Male
Sturge-Weber Syndrome - diagnostic imaging
Sturge-Weber Syndrome - physiopathology
Title Sturge-Weber syndrome: about a case
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Volume 36
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