📂 الأمراض
autosomal recessive congenital ichthyosis 5 — التعريف
Otozomal resesif konjenital iktiyoz 5 / autosomal recessive congenital ichthyosis 5
Otozomal resesif congenital iktiyoz 5 is a rare genetic disease characterized by excessive dryness, exfoliation and fishening in the skin. This condition is caused by gene mutations that lead to disruption of the skin barrier, and is often pronounced in birth or early infancy. The disease manifests itself with the appearance of fish flakes, which affect the large regions of the body, and can often accompanied additional findings such as extropion (external circulation of eyelids).
الأسئلة الشائعة
❓ ما هو Otozomal resesif konjenital iktiyoz 5؟
Otozomal resesif konjenital iktiyoz 5; otozomal resesif congenital iktiyoz 5 is a rare genetic disease characterized by excessive dryness, exfoliation and fishening in the skin. This condition is caused by gene mutations that lead to disruption of the skin barrier, and is often pronounced in birth or early infancy. The disease manifests itself with the appearance of fish flakes, which affect the large regions of the body, and can often accompanied additional findings such as extropion (external circulation of eyelids).
❓ ما معنى autosomal recessive congenital ichthyosis 5 بالتركية؟
المعادل التركي لـ "autosomal recessive congenital ichthyosis 5" هو Otozomal resesif konjenital iktiyoz 5.
❓ ما هو المجال الطبي الذي يتعلق بـ Otozomal resesif konjenital iktiyoz 5؟
هذا المصطلح ينتمي إلى فئة الأمراض.