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  2. Rifampicin - Wikipedia

    en.wikipedia.org/wiki/Rifampicin

    In August 2020, the U.S. Food and Drug Administration (FDA) became aware of nitrosamine impurities in certain samples of rifampin. [61] The FDA and manufacturers are investigating the origin of these impurities in rifampin, and the agency is developing testing methods for regulators and industry to detect the 1-methyl-4-nitrosopiperazine (MNP ...

  3. Category:Autosomal recessive disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Autosomal...

    A. Abdallat–Davis–Farrage syndrome; Abetalipoproteinemia; Absent tibia-polydactyly-arachnoid cyst syndrome; Acanthosis nigricans-muscle cramps-acral enlargement syndrome

  4. Prevention of autosomal recessive disorders - Wikipedia

    en.wikipedia.org/wiki/Prevention_of_autosomal...

    Autosomal recessive pattern, showing how two unaffected carriers can have a child with the disease. Some genetic disorders are caused by having two "bad" copies of a recessive allele. When the gene is located on an autosome (as opposed to a sex chromosome), it is possible for both men and women to be carriers .

  5. Rifamycin - Wikipedia

    en.wikipedia.org/wiki/Rifamycin

    The rifamycin group includes the classic rifamycin drugs as well as the rifamycin derivatives rifampicin (or rifampin), rifabutin, rifapentine, rifalazil and rifaximin. Rifamycin, sold under the trade name Aemcolo, is approved in the United States for treatment of travelers' diarrhea in some circumstances. [1] [2] [3]

  6. Pseudohypoaldosteronism - Wikipedia

    en.wikipedia.org/wiki/Pseudohypoaldosteronism

    Autosomal dominant or autosomal recessive Mean age at diagnosis was found to be around 24 to 26, but it varies widely. [15] May involve salt wasting. [16] Individuals with the autosomal dominant mutations typically show higher potassium levels than those with autosomal recessive mutations. Hypertension usually develops in adulthood.

  7. Multiple sulfatase deficiency - Wikipedia

    en.wikipedia.org/wiki/Multiple_sulfatase_deficiency

    Multiple sulfatase deficiency (MSD), also known as Austin disease, [1] or mucosulfatidosis, [1] is a very rare autosomal recessive [2] lysosomal storage disease [3] caused by a deficiency in multiple sulfatase enzymes, or in formylglycine-generating enzyme, which activates sulfatases. [4]: 502 [5] It is similar to mucopolysaccharidosis. [6]

  8. Alagille syndrome - Wikipedia

    en.wikipedia.org/wiki/Alagille_syndrome

    The "autosomal" aspect of the disease means that the gene mutation occurs in an autosome, which is one of the 44 chromosomes in the human body that is not a sex chromosome (chromosome X or Y). Although the majority of cases are due to the autosomal dominant gene, there have been reports of a rare, autosomal recessive version of the disease. [16]

  9. Giant axonal neuropathy - Wikipedia

    en.wikipedia.org/wiki/Giant_axonal_neuropathy

    This disease is an autosomal recessive disorder, which means the defective gene is located on an autosome, and both parents must have one copy of the defective gene in order to have a child born with the disorder. The parents of a child with an autosomal recessive disorder are carriers, but are usually not affected by the disorder. [citation ...