📂 الأمراض
retinitis pigmentosa 17 — التعريف
Retinitis Pigmentosa 17 / retinitis pigmentosa 17
Retinitis pigmentosa is a genetic disease that causes the progressive degeneration of photoreceptor cells in the retina of the eye. This situation starts especially with night blindness and peripheral vision loss and can lead to full blindness by affecting the central vision over time. The disease manifests autozomal dominant inheritance and is associated with mutations in PRPF31 gene, also known as RP17.
الأسئلة الشائعة
❓ ما هو Retinitis Pigmentosa 17؟
Retinitis Pigmentosa 17; retinitis pigmentosa is a genetic disease that causes the progressive degeneration of photoreceptor cells in the retina of the eye. This situation starts especially with night blindness and peripheral vision loss and can lead to full blindness by affecting the central vision over time. The disease manifests autozomal dominant inheritance and is associated with mutations in PRPF31 gene, also known as RP17.
❓ ما معنى retinitis pigmentosa 17 بالتركية؟
المعادل التركي لـ "retinitis pigmentosa 17" هو Retinitis Pigmentosa 17.
❓ ما هو المجال الطبي الذي يتعلق بـ Retinitis Pigmentosa 17؟
هذا المصطلح ينتمي إلى فئة الأمراض.