Exfoliation syndrome

MONDO:0008327

An autosomal dominant disorder caused by mutations in the LOXL1 gene, encoding lysyl oxidase homolog 1. The condition is characterized by abnormal fibrillar extracellular material in anterior segment tissues, and may lead to glaucoma.

Also known as: XFG, XFS, pseudoexfoliation glaucoma

40 clinical trials for this condition and its sub-types.

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