PSC (primary sclerosing cholangitis)
Primary sclerosing cholangitis.
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A rare genetic disease that is passed on via an autosomal recessive gene. It is characterized by abnormal lysosomal enzyme transport in cells of mesenchymal origin, causing elevated lysosomal enzymes in body fluids and tissues. Diagnosis is by blood test. There is currently no treatment for this disorder. Also known as mucolipidosis III.
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Inflammation of the joints that is caused by deposits of calcium pyrophosphate crystals, resulting in arthritis, most commonly of the knees, wrists, shoulders, hips, and ankles. Pseudogout usually affects only one or a few joints at a time. True gout is due to a different type of crystal, which is formed by the precipitation of […]
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