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porphyria |
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porphyriaGroup of rare genetic disorders caused by an enzyme defect. Porphyria affects the digestive tract, causing abdominal distress; the nervous system, causing psychotic disorder, epilepsy, and weakness; the circulatory system, causing high blood pressure; and the skin, causing extreme sensitivity to light. No specific treatments exist. In porphyria the body accumulates and excretes (rather than utilizes) one or more porphyrins, the pigments that combine with iron to form part of the oxygen-carrying proteins haemoglobin and myoglobin; because of this urine turns reddish brown on standing. It is sometimes known as the ‘royal disease’ because sufferers are believed to have included Mary Queen of Scots, James I, and George III. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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Coproporphyrinuria and chronic hepatic porphyria Type A found in farm families from Michigan (U. 1986), characterized by hepatic porphyria and cutaneous skin lesions caused by a disturbed porphyrin metabolism (Bickers 1987). One of the earliest features of griseofulvin exposure is a hepatic porphyria characterized by the accumulation of protoporphyrin IX (De Matteis and Rimington 1963; Weston Hurst and Paget 1963). |
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