Pochopení blefarofimózy: příčiny, příznaky a možnosti léčby

Blefarofimóza je vzácná genetická porucha, která postihuje oční víčka a může způsobit řadu příznaků, včetně pokleslých víček, potíží s úplným zavřením očí a problémů se zrakem. Je způsobena mutacemi v genu FOXC1 a je obvykle zděděna autozomálně dominantním vzorem. Treatment options for blepharophimosis may include surgery to correct the position of the eyelids, glasses or contact lenses to improve vision, and other supportive measures to address any associated symptoms.

CRISPRITICKNOWNEYRARREROLEGY

CRISPRITICKNOWNEYRARREROLEGY

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