Cerebral folate deficiency: Difference between revisions
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File:5-Methyltetrahydrofolate.png|5-Methyltetrahydrofolate | |||
File:Cerebral Folate Deficiency - Cerebral CT-scan at 4 years old.png|Cerebral Folate Deficiency - Cerebral CT-scan at 4 years old | |||
File:Folic acid metabolism and 5-MTHF transport across the choroid plexus epithelium in the brain.png|Folic acid metabolism and 5-MTHF transport across the choroid plexus epithelium in the brain | |||
File:Transport of folate compounds from the intestine to the brain and competitive inhibition of 5-MTHF transport by folic acid.png|Transport of folate compounds from the intestine to the brain and competitive inhibition of 5-MTHF transport by folic acid | |||
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Latest revision as of 00:35, 20 February 2025
| Cerebral Folate Deficiency | |
|---|---|
| Synonyms | N/A |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Developmental delay, movement disorders, seizures |
| Complications | Intellectual disability, autism spectrum disorder |
| Onset | Infancy |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutations, autoimmunity |
| Risks | N/A |
| Diagnosis | CSF analysis, genetic testing |
| Differential diagnosis | N/A |
| Prevention | N/A |
| Treatment | Folinic acid supplementation |
| Medication | N/A |
| Prognosis | N/A |
| Frequency | Rare |
| Deaths | N/A |
Cerebral Folate Deficiency (CFD) is a neurological disorder characterized by low levels of 5-methyltetrahydrofolate (5-MTHF) in the cerebrospinal fluid (CSF) despite normal levels of folate in the blood. This condition can lead to a variety of neurological symptoms and developmental issues.
Signs and Symptoms[edit]
Individuals with cerebral folate deficiency may present with a range of symptoms, including:
- Developmental delay
- Movement disorders
- Seizures
- Ataxia
- Spasticity
- Autism spectrum disorder
- Intellectual disability
Causes[edit]
Cerebral folate deficiency can be caused by several factors, including:
- Genetic mutations affecting folate transport, such as mutations in the FOLR1 gene.
- Autoimmune disorders where antibodies interfere with folate transport across the blood-brain barrier.
- Secondary causes such as mitochondrial disorders or cerebral palsy.
Diagnosis[edit]
Diagnosis of cerebral folate deficiency typically involves:
- Analysis of 5-MTHF levels in the cerebrospinal fluid through a lumbar puncture.
- Genetic testing to identify mutations in genes related to folate transport.
- Testing for the presence of folate receptor autoantibodies.
Treatment[edit]
The primary treatment for cerebral folate deficiency is supplementation with folinic acid, which can help increase the levels of 5-MTHF in the CSF and alleviate symptoms. Early diagnosis and treatment are crucial for improving outcomes.
Prognosis[edit]
The prognosis for individuals with cerebral folate deficiency varies depending on the underlying cause and the timeliness of treatment. With appropriate management, some symptoms can be improved, but developmental delays and neurological impairments may persist.
See Also[edit]
References[edit]
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External Links[edit]
Template:Medical condition (neurology)
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5-Methyltetrahydrofolate
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Cerebral Folate Deficiency - Cerebral CT-scan at 4 years old
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Folic acid metabolism and 5-MTHF transport across the choroid plexus epithelium in the brain
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Transport of folate compounds from the intestine to the brain and competitive inhibition of 5-MTHF transport by folic acid