Hereditary folate malabsorption

From WikiMD's Wellness Encyclopedia

Hereditary Folate Malabsorption
Synonyms N/A
Pronounce N/A
Specialty N/A
Symptoms Anemia, Diarrhea, Seizures, Developmental delay
Complications N/A
Onset Infancy
Duration Lifelong
Types N/A
Causes Genetic mutation in the SLC46A1 gene
Risks N/A
Diagnosis Blood test, Genetic testing
Differential diagnosis N/A
Prevention N/A
Treatment Folate supplementation
Medication N/A
Prognosis Variable
Frequency N/A
Deaths N/A


Hereditary Folate Malabsorption is a rare genetic disorder characterized by the body's inability to absorb folate from the diet. This condition is caused by mutations in the SLC46A1 gene, which encodes the proton-coupled folate transporter (PCFT) responsible for the absorption of folate in the small intestine.

Signs and Symptoms[edit | edit source]

Individuals with hereditary folate malabsorption typically present with symptoms in infancy. Common symptoms include:

Causes[edit | edit source]

The condition is caused by mutations in the SLC46A1 gene. This gene provides instructions for making a protein that transports folate across cell membranes. Mutations in this gene disrupt the function of the protein, leading to reduced absorption of folate from the diet.

Diagnosis[edit | edit source]

Diagnosis of hereditary folate malabsorption is based on clinical evaluation, laboratory tests, and genetic testing. Blood tests may reveal low levels of folate, and genetic testing can identify mutations in the SLC46A1 gene.

Treatment[edit | edit source]

Treatment involves lifelong folate supplementation to bypass the defective absorption mechanism. High doses of oral folate or intravenous folate may be required to maintain adequate levels in the body.

Prognosis[edit | edit source]

The prognosis for individuals with hereditary folate malabsorption varies. Early diagnosis and treatment can improve outcomes and prevent complications such as neurological damage.

See Also[edit | edit source]

References[edit | edit source]


External Links[edit | edit source]

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Contributors: Prab R. Tumpati, MD