📂 Diseases
congenital disorder of glycosylation Ij — Definition
Glikozilasyon Tip Ij Konjenital Bozukluğu / congenital disorder of glycosylation Ij
Glycosilation Type 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. The disease often states during pregnancy and is a condition that lasts for life.
Frequently Asked Questions
❓ What is Glikozilasyon Tip Ij Konjenital Bozukluğu?
Glikozilasyon Tip Ij Konjenital Bozukluğu; glycosilation Type 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. The disease often states during pregnancy and is a condition that lasts for life.
❓ What is congenital disorder of glycosylation Ij in Turkish?
The Turkish equivalent of "congenital disorder of glycosylation Ij" is Glikozilasyon Tip Ij Konjenital Bozukluğu.
❓ Which medical field is Glikozilasyon Tip Ij Konjenital Bozukluğu related to?
This term belongs to the Diseases category.