Définition: A congenital syndrome characterized by a port-wine nevus covering portions of the face and cranium (in the distribution of the ophthalmic division of the TRIGEMINAL NERVE) and angiomas of the meninges and choroid. Clinical manifestations include the onset of focal SEIZURES, progressive hemiparesis, GLAUCOMA, hemianopsia, and cognitive deficits in the first decade of life. By age two years, skull radiographs reveal "tramline calcifications" of the margins of the occipital and parietal lobes. Pathologically cortical neurons are replaced by glial tissue that undergoes calcification. (From Adams et al., Principles of Neurology, 6th ed, pp1018-9) Synonyme(s): Angiomatose encéphalotrigéminée / Angiomatose congénitale de Sturge-Weber-Krabbe / Maladie de Sturge-Weber-Krabbe / Phacomatose de Sturge-Weber-Krabbe /
Termes généraux: - Hémangiome - Tumeurs - Syndromes néoplasiques héréditaires - Syndromes neurocutanés - Maladies du système nerveux - Angiomatose - Maladies vasculaires - Maladies cardiovasculaires
Qualificatifs: épidémiologie / étiologie / chirurgie / complications / diagnostic / embryologie / metabolisme / microbiologie / thérapeutique
Termes généraux: - Hémangiome - Tumeurs - Syndromes neurocutanés - Maladies du système nerveux - Angiomatose - Maladies vasculaires - Maladies cardiovasculaires
Termes généraux: - Maladies cardiovasculaires