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  2. Methylenetetrahydrofolate reductase - Wikipedia

    en.wikipedia.org/wiki/Methylenetetrahydrofolate...

    In studies of human recombinant MTHFR, the protein encoded by 1298C cannot be distinguished from 1298A in terms of activity, thermolability, FAD release, or the protective effect of 5-methyl-THF. [22] The C mutation does not appear to affect the MTHFR protein. It does not result in thermolabile MTHFR and does not appear to affect homocysteine ...

  3. Methylenetetrahydrofolate reductase deficiency - Wikipedia

    en.wikipedia.org/wiki/Methylenetetrahydrofolate...

    MTHFR is the rate-limiting enzyme in the methyl cycle, which includes the conversion of homocysteine into methionine. Defects in variants of MTHFR can therefore lead to hyperhomocysteinemia. [9] There are two common variants of MTHFR deficiency. In the more significant of the two, the individual is homozygous for the 677T polymorphism.

  4. Cerebral folate deficiency - Wikipedia

    en.wikipedia.org/wiki/Cerebral_folate_deficiency

    For people with the FOLR1 mutation, even when the systemic deficiency is corrected by folate, the cerebral deficiency remains and must be treated with folinic acid. Success depends on early initiation of treatment and treatment for a long period of time. [9] [3] Fewer than 20 people with the FOLR1 defect have been described in the medical ...

  5. rs1801133 - Wikipedia

    en.wikipedia.org/wiki/Rs1801133

    C677T or rs1801133 is a genetic variation—a single nucleotide polymorphism (SNP)—in the MTHFR gene. Among Americans the frequency of T-homozygosity ranges from 1% or less among people of sub-Saharan African descent to 20% or more among Italians and Hispanics. [1] It has been related to schizophrenia [2] Alzheimer's disease [3] depression [4 ...

  6. 5,10-methenyltetrahydrofolate synthetase deficiency - Wikipedia

    en.wikipedia.org/wiki/5,10-methenyltetrahydrofo...

    5,10-Methenyltetrahydrofolate synthetase deficiency (MTHFS deficiency) is a rare neurodevelopmental disorder caused by mutations affecting the MTHFS gene, which encodes the enzyme 5,10-Methenyltetrahydrofolate synthetase. [2] The disease starts at birth or in early infancy and presents with microcephaly, short stature, and developmental delay.

  7. List of medical roots, suffixes and prefixes - Wikipedia

    en.wikipedia.org/wiki/List_of_medical_roots...

    This is a list of roots, suffixes, and prefixes used in medical terminology, their meanings, and their etymologies. Most of them are combining forms in Neo-Latin and hence international scientific vocabulary. There are a few general rules about how they combine.

  8. This Christmas, ask for genetic testing. It could save your life.

    www.aol.com/christmas-ask-genetic-testing-could...

    Rose Brystowski, 68, had a choice to make. Others might have found it difficult. She found it easy. Brystowski, of Oak Park, Michigan, wasn't about to let her genetics forfeit her future. Doctors ...

  9. Talk:Methylenetetrahydrofolate reductase - Wikipedia

    en.wikipedia.org/wiki/Talk:Methylenetetrahydrofo...

    MTHFR = methelynetetrahydrofolate reductase; MTHF = Methyltetrahydrofolate. Without the effective reductase action, your body can't make enough of the folate form. You also won't have an efficient methylization cycle to clean up all kinds of junk in your body. Work with your medical doctor to test for MTHFR defects and appropriate supplementation.