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• W2007763306 abstract "Alagille syndrome is an autosomal dominant condition with incomplete penetrance that is associated mostly with hepatic, cardiac, and skeletal abnormalities. In addition, the association of Alagille syndrome with ocular abnormalities is well known and is considered one of the characteristic features of this condition. Most commonly, posterior embryotoxon, glaucoma, or retinopathy has been identified in these children. The authors present 2 patients with Alagille syndrome who, before the age of 3 years old, developed idiopathic intracranial hypertension with documented increased intracranial pressure by lumbar puncture and papilledema, which was responsive to acetazolamide." @default.
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• W2007763306 date "2010-05-25" @default.
• W2007763306 modified "2023-09-25" @default.
• W2007763306 title "Idiopathic Intracranial Hypertension in Two Patients With Alagille Syndrome" @default.
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• W2007763306 doi "https://doi.org/10.1177/0883073809351985" @default.
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