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  2. Hereditary haemochromatosis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_haemochromatosis

    A study of 3,011 unrelated white Australians found that 14% were heterozygous carriers of an HFE mutation, 0.5% were homozygous for an HFE mutation, and only 0.25% of the study population had clinically relevant iron overload. Most patients who are homozygous for HFE mutations do not manifest clinically relevant haemochromatosis (see Genetics ...

  3. Canine transmissible venereal tumor - Wikipedia

    en.wikipedia.org/wiki/Canine_transmissible...

    Dog cells normally have 78 chromosomes, while the cancer cells contain 57–64 chromosomes [9] that are very different in appearance from normal dog chromosomes. All dog chromosomes except X and Y are acrocentric, having a centromere very near to the end of the chromosome, while many of the CTVT chromosomes are metacentric or submetacentric ...

  4. Multiple myeloma - Wikipedia

    en.wikipedia.org/wiki/Multiple_myeloma

    Multiple myeloma has been diagnosed in dogs, [157] cats, and horses. [158] In dogs, multiple myeloma accounts for around 8% of all haemopoietic tumors. Multiple myeloma occurs in older dogs and is not particularly associated with either males or females. No breeds appear overrepresented in case reviews that have been conducted. [159]

  5. Urine cytology - Wikipedia

    en.wikipedia.org/wiki/Urine_cytology

    The Paris System for reporting urine cytology, version 2.0, ranging from negative to positive for high grade urothelial carcinoma. [1] Urine cytology is a test that looks for abnormal cells in urine under a microscope. The test commonly checks for infection, inflammatory disease of the urinary tract, cancer, or precancerous conditions.

  6. Genetic testing - Wikipedia

    en.wikipedia.org/wiki/Genetic_testing

    A blood sample is collected with a heel prick from the newborn 24–48 hours after birth and sent to the lab for analysis. In the United States, newborn screening procedure varies state by state, but all states by law test for at least 21 disorders. If abnormal results are obtained, it does not necessarily mean the child has the disorder.

  7. Cystinosis - Wikipedia

    en.wikipedia.org/wiki/Cystinosis

    Cystinosis is a rare genetic disorder [11] that causes an accumulation of the amino acid cystine within cells, forming crystals that can build up and damage the cells. These crystals negatively affect many systems in the body, especially the kidneys and eyes. [3]

  8. Hematuria - Wikipedia

    en.wikipedia.org/wiki/Hematuria

    Hematuria can be classified according to visibility, anatomical origin, and timing of blood during urination. [1] [6]In terms of visibility, hematuria can be visible to the naked eye (termed "gross hematuria") and may appear red or brown (sometimes referred to as tea-colored), or it can be microscopic (i.e. not visible but detected with a microscope or laboratory test).

  9. Methylmalonic acidemias - Wikipedia

    en.wikipedia.org/wiki/Methylmalonic_acidemias

    For baseline, collect urine from 3 different days. Blood plasma concentrations can also be used if test is sensitive enough. Intramuscular injection of 1 mg hydroxocobalamin on 3 consecutive days. After injection, collect urine or plasma samples on alternate days for 10 days. The urine or plasma samples should be analyzed in the same run by GCMS.