B3GALT6-congenital disorder of glycosylation

B3GALT6-congenital disorder of glycosylation is a rare inherited condition that occurs because of a mutation in the B3GALT6 gene. This mutation affects the glycosylation process, which is important for many functions in the body. This disorder is part of a group of conditions known as congenital disorders of glycosylation. The mutation disrupts normal cell function, leading to a range of potential challenges. Information specific to the range of symptoms and severity is currently limited for this condition.

Information about symptoms is currently limited for this condition.

B3GALT6-congenital disorder of glycosylation is caused by a mutation in the B3GALT6 gene. This mutation affects the process of glycosylation, which is needed for normal biological functions in the body.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about current research is currently limited for this condition.