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Approximately half of the psammomatous cases are associated with CC, an autosomal dominant genetic disease harboring a chromosome 17 mutation that affects the cAMP-dependent protein kinase type I regulatory subunit alpha ( PRKAR1A ) gene (42)

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Advertisement Certain populations are at increased risk of uveitis: people with a family history of uveitis, people with a genetic predisposition to uveitis and people with autoimmune disease, Mohan says