📂 الأمراض
congenital disorder of glycosylation Ij — التعريف
Glikozilasyon Tip Ij Konjenital Bozukluğu / congenital disorder of glycosylation Ij
نوع الترميز Ij congenital disorder is a rare disease caused by a genetic defect that provides proper sugaring (glucosilation) of proteins and fats in the body. This disorder leads to a variety of clinical symptoms, such as neurological development backrest, liver problems and immune system weakness. وكثيراً ما يُذكر المرض أثناء الحمل، وهو شرط يدوم مدى الحياة.
الأسئلة الشائعة
❓ ما هو Glikozilasyon Tip Ij Konjenital Bozukluğu؟
Glikozilasyon Tip Ij Konjenital Bozukluğu; نوع الترميز Ij congenital disorder is a rare disease caused by a genetic defect that provides proper sugaring (glucosilation) of proteins and fats in the body. This disorder leads to a variety of clinical symptoms, such as neurological development backrest, liver problems and immune system weakness. وكثيراً ما يُذكر المرض أثناء الحمل، وهو شرط يدوم مدى الحياة.
❓ ما معنى congenital disorder of glycosylation Ij بالتركية؟
المعادل التركي لـ "congenital disorder of glycosylation Ij" هو Glikozilasyon Tip Ij Konjenital Bozukluğu.
❓ ما هو المجال الطبي الذي يتعلق بـ Glikozilasyon Tip Ij Konjenital Bozukluğu؟
هذا المصطلح ينتمي إلى فئة الأمراض.