Porphyria is a group of hereditary diseases associated with impaired porphyrin metabolism. This can lead to a variety of symptoms, including porphyrins in the urine, increased sensitivity to sunlight, and nerve inflammation. One of the most common types of porphyria is porphyria tarda, which affects about 1% of the population. However, porphyria can also be caused by other reasons, such as taking certain medications or alcoholism. Treatment for porphyria may include changing your diet, reducing your stress levels, and using certain medications.
Porphyria is a dire diagnosis that is heard less and less often > There are approximately *50 different forms* of hereditary disorders associated with disruption of normal heme synthesis. The most famous among them is ***hepatic porphyria***. Its variant is ***porphyria tarda
Porphyria is a severe hereditary polysyndromic disease that occurs when hemoglobin synthesis is disrupted in the cells of the hematopoietic system, associated with a deficiency of enzymes of cobalamin-dependent reactions of hydroxylation of protoporphyrin, DNA, carbohydrates, etc. However, damage to kidney cells, gastrointestinal tract, and blood vessels also occurs; central and peripheral nervous system; skin; mucous membranes of the nose and pharynx, paranasal sinuses and lymph nodes, hands, feet and external genitalia. The main site of porphyrin formation is the retinal pigment epithelium. The porphyrins accumulated there in response to irritation, injury, and inflammatory processes are released into the blood, from where they are transferred to all tissues and organs. One of the main targets of this toxin in human tissues and organs is the central nervous system.
Porphyria: a disease that cannot be recognized at first sight.
Porphyria is a rare hereditary disease that is caused by disturbances in the metabolism of hemoglobin breakdown products, porphyrin. More than half of porphyria cases have a genetic cause, although sometimes the condition can occur due to exposure to toxic substances or infections. In Russia, the disease is diagnosed in only one woman out of 10,000