📂 الأمراض
cone-rod dystrophy 21 — التعريف
koni-çubuk distrofisi 21 / cone-rod dystrophy 21
Koni-çubuk dystrophy is a hereditary disease that affects photoreceptor cells (conies and rods) in the retina of the eye. The disease begins with function loss of cone cells especially and leads to visual sharp reduction, color vision disorder and night blindness by also affecting rod cells over time. This form, which shows autozomal resesif, usually manifests in early child or young adulthood period, and can cause severe loss of vision due to its progressive character.
الأسئلة الشائعة
❓ ما هو koni-çubuk distrofisi 21؟
koni-çubuk distrofisi 21; koni-çubuk dystrophy is a hereditary disease that affects photoreceptor cells (conies and rods) in the retina of the eye. The disease begins with function loss of cone cells especially and leads to visual sharp reduction, color vision disorder and night blindness by also affecting rod cells over time. This form, which shows autozomal resesif, usually manifests in early child or young adulthood period, and can cause severe loss of vision due to its progressive character.
❓ ما معنى cone-rod dystrophy 21 بالتركية؟
المعادل التركي لـ "cone-rod dystrophy 21" هو koni-çubuk distrofisi 21.
❓ ما هو المجال الطبي الذي يتعلق بـ koni-çubuk distrofisi 21؟
هذا المصطلح ينتمي إلى فئة الأمراض.