Abstract
Sturge Weber angiomatosis is a rare, nonhereditary developmental condition characterized by a hamartomatous vascular proliferation involving the tissues of brain and face, port wine stains, dilated ocular vessels and glaucoma[1].
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APA
Joshi, R., Bora, B., Jadhav, J., & Mhatre, P. (2016). Sturge weber syndrome-A case report. Pravara Medical Review, 8(2), 25–28. https://doi.org/10.36347/sasjm.2024.v10i09.011
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