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What is congenital disorder of glycosylation cdg?

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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?

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

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