Hamdani M, Rais L, Elbelhadj M, Nejjar N, Laouissi N, Zaghloul K, Hadj Khalifa H, Amraoui A
Hôpital 20-Aout, Centre Hospitalier Ibn Rochd, Casablanca, Maroc.
J Fr Ophtalmol. 1997;20(3):213-6.
We report a case of bilateral Sturge-Weber-Krabbe syndrome. The patient was a child aged 2 years. He presented facial and jugal angioma, bilateral glaucoma and epilepsy. The cerebral scan showed calcifications characterised by their localisations and their aspects. Cure and prognosis of this disease are discussed.
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