A blefarofimózis megértése: okok, tünetek és kezelési lehetőségek

A blefarofimózis egy ritka genetikai rendellenesség, amely a szemhéjakat érinti, és számos tünetet okozhat, beleértve a lógó szemhéjakat, a szemek teljes becsukásának nehézségeit és a látási problémákat. A FOXC1 gén mutációi okozzák, és általában autoszomális domináns mintázatban öröklődnek. 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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