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Up to: Hereditary anemia · Megaloblastic anemia · Disorder of folate metabolism and transport
Formiminoglutamic aciduria
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.
This condition has no sub-types.