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  2. Pentadecylic acid - Wikipedia

    en.wikipedia.org/wiki/Pentadecylic_acid

    Pentadecylic acid, also known as pentadecanoic acid or C15:0, is an odd-chain saturated fatty acid. Its molecular formula is CH 3 (CH 2) 13 CO 2 H. It is a colorless solid. A laboratory preparation involves permanganate oxidation of 1-hexadecene (CH 3 (CH 2) 13 CH=CH 2). [2] It is one of the most common odd-chain fatty acids, although it is ...

  3. Very long-chain acyl-coenzyme A dehydrogenase deficiency

    en.wikipedia.org/wiki/Very_long-chain_acyl...

    VLCAD (very long-chain-acyl-dehydrogenase) deficiency is exclusively linked to genetic mutations in DNA. A change of the gene that codes for very long-chain-acyl-CoA-dehydrogenase (VLCAD) results in a deficiency or malfunction of the produced VLCAD enzyme. [7] This mutation occurs on chromosome 17 and can be altered via a variety of pathways. [4]

  4. Side effects of cyproterone acetate - Wikipedia

    en.wikipedia.org/wiki/Side_effects_of_cyprotero...

    The side effects of cyproterone acetate (CPA), a steroidal antiandrogen and progestin, including its frequent and rare side effects, have been studied and characterized.It is generally well-tolerated and has a mild side-effect profile, regardless of dosage, when it used as a progestin or antiandrogen in combination with an estrogen such as ethinylestradiol or estradiol valerate in women.

  5. Carnitine-acylcarnitine translocase deficiency - Wikipedia

    en.wikipedia.org/wiki/Carnitine-acylcarnitine...

    Carnitine-acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long-chain fatty acids into energy, particularly during periods without food. [1] Carnitine, a natural substance acquired mostly through the diet, is used by cells to process fats and produce energy.

  6. Methylmalonic acidemias - Wikipedia

    en.wikipedia.org/wiki/Methylmalonic_acidemias

    Methylmalonic acidemias have varying diagnoses, treatment requirements and prognoses, which are determined by the specific genetic mutation causing the inherited form of the disorder. [3] The first symptoms may begin as early as the first day of life or as late as adulthood. [4] Symptoms can range from mild to life-threatening. [1]

  7. Glucocorticoid deficiency - Wikipedia

    en.wikipedia.org/wiki/Glucocorticoid_deficiency

    With appropriate treatment, most individuals with glucocorticoid deficiency can lead normal lives and have a good prognosis. [4] However, it is important to closely monitor hormone levels and adjust medication accordingly to prevent complications such as adrenal crisis or over-replacement side effects. [1]

  8. Common variable immunodeficiency - Wikipedia

    en.wikipedia.org/wiki/Common_variable...

    This treatment replenishes Ig subtypes that the person lacks, is given at frequent intervals for life, and is thought to help reduce bacterial infections and boost immune function. [25] Before therapy begins, plasma donations are tested for known blood-borne pathogens, then pooled and processed to obtain concentrated IgG samples.

  9. Holocarboxylase synthetase deficiency - Wikipedia

    en.wikipedia.org/wiki/Holocarboxylase_synthetase...

    Holocarboxylase synthetase deficiency is an inherited metabolic disorder in which the body is unable to use the vitamin biotin effectively. [2] This disorder is classified as a multiple carboxylase deficiency , a group of disorders characterized by impaired activity of certain enzymes that depend on biotin.