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Is Glutaryl-CoA dehydrogenase deficiency / Glutaric aciduria type 1 hereditary?
Here you can see if Glutaryl-CoA dehydrogenase deficiency / Glutaric aciduria type 1 can be hereditary. Do you have any genetic components? Does any member of your family have Glutaryl-CoA dehydrogenase deficiency / Glutaric aciduria type 1 or may be more predisposed to developing the condition?
Yes, Glutaryl-CoA dehydrogenase deficiency, also known as Glutaric aciduria type 1, is a hereditary condition. It is caused by mutations in the GCDH gene, which is inherited in an autosomal recessive manner. This means that both parents must carry a copy of the mutated gene for their child to be affected. Early diagnosis and treatment are crucial to manage this metabolic disorder and prevent potential complications.
