Summary Congenital disorders of glycosylation (CDG) is an umbrella term for a rapidly expanding group of rare genetic, metabolic disorders due to defects in complex chemical process known as glycosylation.
What is CDG? CDG stands for Congenital Disorders of Glycosylation. CDG is a large group of rare inherited diseases affecting glycosylation.
What is Congenital Disorder of Glycosylation Type 1a? Congenital disorder of glycosylation type 1a (CDG-1a) is an inherited disease characterized by variable developmental delays and muscle and bone problems that change with age. It involves defects in the enzyme
Please let the audience know your advice: