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Arakawa syndrome 2

rare

A rare autosomal dominant inherited metabolic disorder characterized by deficiency of the enzyme tetrahydrofolate-methyltransferase. It results in the abnormal metabolism of methylcobalamin. Signs and symptoms include mental retardation, megaloblastic anemia, hypotonia, epilepsy, and hepatosplenomegaly.

Identifiers
MONDO:0021915
Also known as
Arakawa syndrome II · Arakawa's syndrome 2 · Arakawa's syndrome II · homocystinuria-megaloblastic Anemia, cblG complementation type · methionine synthase deficiency

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