Hereditary folate malabsorption

Hereditary folate malabsorption (HFM) is an inherited disorder of folate transport characterized by a systemic and central nervous system (CNS) folate deficiency manifesting as megaloblastic anemia, failure to thrive, diarrhea and/or oral mucositis, immunologic dysfunction and neurological disorders.

Also known as: congenital folate malabsorption, congenital defect of folate absorption, folate malabsorption, hereditary, folic acid transport defect

69 clinical trials for this condition and its sub-types.