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Formiminoglutamic aciduria

rare

Formiminoglutamic aciduria, in its moderate form and in the absence of histidine administration, is characterized by mild developmental delay and elevated concentrations of formiminoglutamate (FIGLU) in the urine. A more severe phenotype has been described in five members of a Japanese family and included severe intellectual deficit, psychomotor retardation and megaloblastic anemia.

Causal genes
FTCD
Also known as
Arakawa syndrome 1 · formiminoglutamic acidemia · Formiminoglutamicaciduria (FIGLU-Uria) · formiminotransferase cyclodeaminase deficiency · formiminotransferase deficiency syndrome

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