Porphyria
Any of a group of inherited diseases characterized by skin sensitivity to sunlight and/or by intermittent acute attacks of abdominal and nerve pain. The porphyrias are caused by enzyme defects that trigger the overproduction of porphyrins by the bone marrow or liver. (Enzymes are proteins that control the speed of chemical reactions in the body. Porphyrins are chemical compounds that the body combines with iron to make heme, a blood component that transports oxygen to tissues throughout the body.) Not all persons with porphyria experience acute attacks. In those that do suffer them, the attack may range from mild to severe. Besides abdominal and nerve pain, the victim may suffer rapid heartbeat, mania, muscle cramps, muscle weakness, breathing problems, hallucinations and coma. Acute attacks are often precipitated by the following: {{}}The use of certain drugs such as barbiturates, sulphonamides and birth-control pills; Alcohol use; Hormonal changes during menstruation or pregnancy; Dieting or fasting; and Infections. Diagnosis requires a thorough physical exam and laboratory tests that include analysis of blood, urine, and stools. Treatment involves appropriate measures to relieve symptoms. A high-carbohydrate diet and avoidance of precipitating factors, wherever possible, can help patients reduce their risk of suffering an acute attack. Severe acute attacks may require hospitalization to stabilize the patient, relieve pain and monitor the body's fluid levels.
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A group of disorders involving heme biosynthesis, characterized by excessive excretion of porphyrins or their precursors; may be inherited or may be acquired, as from the effects of certain chemical agents ( e.g., hexachlorobenzene).
- δ-aminolevulinate dehydratase p. an inherited disorder in which there is a deficiency of porphobilinogen synthase; δ-aminolevulinate levels are elevated, leading to neurologic disturbances. SYN: porphobilinogen synthase p..
- congenital erythropoietic p. [MIM*263700] enhanced porphyrin formation by erythroid cells in bone marrow, leading to severe porphyrinuria, often with hemolytic anemia and persistent cutaneous photosensitivity; caused by a deficiency of uroporphyrinogen III cosynthetase; autosomal recessive inheritance, caused by mutation in the uroporphyrinogen III synthase gene (UROS) on chromosome 10q; there is an overproduction of type I porphyrin isomers.
- p. cutanea tarda (PCT) [MIM*176090, MIM*176100] familial or sporadic p. characterized by liver dysfunction and photosensitive cutaneous lesions, with bullae, hyperpigmentation, and scleroderma-like changes in the skin and increased excretion of uroporphyrin; caused by a deficiency of uroporphyrinogen decarboxylase induced in sporadic cases by chronic alcoholism; autosomal dominant inheritance in familial cases. SYN: symptomatic p..
- p. cutanea tarda hereditaria See p. cutanea tarda.
- p. cutanea tarda symptomatica See p. cutanea tarda.
- hepatic p. [MIM*176100.0002] a category of p. that includes p. cutanea tarda, variegate p., and coproporphyria. SYN: p. hepatica.
- p. hepatica (he-pat′i-ka) SYN: hepatic p..
- hepatoerythropoietic p. an autosomal recessive disorder in which there is a deficiency or absence of uroporphyrinogen decarboxylase; results in photosensitivity and excessive hepatic production of 8- and 7-carboxylate porphyrins.
- intermittent acute p. (IAP) [MIM*176000] p. caused by hepatic overproduction of δ-aminolevulinic acid, with greatly increased urinary excretion of it and of porphobilinogen, and some increase of uroporphyrin, due to a deficiency of porphobilinogen deaminase; characterized by intermittent acute attacks of hypertension, abdominal colic, psychosis, and polyneuropathy, but with no photosensitivity; autosomal dominant inheritance, caused by mutation in the human porphobilinogen deaminase gene on 11q24; exacerbation caused by ingestion of certain drugs ( e.g., barbiturates). SYN: acute intermittent p., acute p..
- ovulocyclic p. acute episodic exacerbations of p. occurring in the premenstrual period.
- porphobilinogen synthase p. SYN: δ-aminolevulinate dehydratase p..
- South African type p. SYN: variegate p..
- symptomatic p. SYN: p. cutanea tarda.
- variegate p. (VP) [MIM*176200] p. characterized by abdominal pain and neuropsychiatric abnormalities, by dermal sensitivity to light and mechanical trauma, by increased fecal excretion of proto- and coproporphyrin, and by increased urinary excretion of δ-aminolevulinic acid, porphobilinogen, and porphyrins; due to a deficiency of protoporphyrinogen oxidase; autosomal dominant inheritance, caused by mutation in the gene for protoporphyrinogen oxidase (PPOX) on chromosome 1q. SYN: protocoproporphyria hereditaria, South African type p..

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por·phyr·ia pȯr-'fir-ē-ə n any of several usu. hereditary abnormalities of porphyrin metabolism characterized by excretion of excess porphyrins in the urine and by extreme sensitivity to light

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n.
one of a group of rare disorders due to inborn error of metabolism in which there are deficiencies in the enzymes involved in the biosynthesis of haem. The accumulation of the enzyme's substrate gives rise to symptoms of the disorder. The defect may be primarily in the liver (hepatic porphyria) or in the bone marrow (erythropoietic porphyria) or both. The prominent features include the excretion of porphyrin and their derivatives in the urine, which may change colour on standing (see porphobilinogen); sensitivity of the skin to sunlight causing chronic inflammation or blistering; inflammation of the nerves (neuritis); mental disturbances; and attacks of abdominal pain. The commonest porphyria is porphyria cutanea tarda, which affects up to 1 in 5000 people in some countries. It is a hereditary or acquired hepatic porphyria in which light-exposed areas of the skin become blistered and fragile. Acute intermittent porphyria is a hereditary hepatic porphyria characterized by recurrent attacks of acute abdominal pain, severe constipation, and psychotic behaviour. Factors triggering attacks include alcohol and many drugs.

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por·phy·ria (por-fērґe-ə) [Gr. porphyra purple] any of a group of disturbances of porphyrin metabolism, characterized biochemically by marked increase in formation and excretion of porphyrins or their precursors and clinically by various neurologic and cutaneous manifestations. The types are generally classified as hepatic, erythropoietic, and sometimes erythrohepatic, depending on the location of expression of the biochemical defect.

Medical dictionary. 2011.

Look at other dictionaries:

  • porphyria — porphyria. См. порфирии. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …   Молекулярная биология и генетика. Толковый словарь.

  • porphyria — 1923, from porphyrin (1910), from Ger. porphyrin, chemical name, from Gk. porphyros “purple” (see PURPLE (Cf. purple)) + IN (Cf. in) (2). Some of the compounds are purple …   Etymology dictionary

  • porphyria — [pôr fir′ē ə] n. [ModL < PORPHYRIN + IA] an inherited disorder of pigment metabolism with excretion of porphyrins in the urine and dangerous sensitivity to sunlight …   English World dictionary

  • Porphyria — This article is about the medical condition. For other uses, see Porphyry (disambiguation). Porphyria Classification and external resources ICD 10 E80.0 E80.2 …   Wikipedia

  • porphyria — /pawr fear ee euh, fuy ree euh/, n. Pathol. a defect of blood pigment metabolism in which porphyrins are produced in excess, are present in the blood, and are found in the urine. Also called hematoporphyria. [1920 25; PORPHYR(IN) + IA] * * * ▪… …   Universalium

  • porphyria — n. one of a group of rare disorders due to inborn errors of metabolism in which there are deficiencies in the enzymes involved in the biosynthesis of haem. The accumulation of the enzyme s substrate gives rise to symptoms of the disorder. The… …   The new mediacal dictionary

  • Porphyria — (Poor FEAR ee ah) Porphyria is a rare hereditary medical condition in which a person s body does not produce heme, the main component in hemoglobin. Those who suffer with this disease have a sensitivity to sunlight, allergic reactions to GARLIC,… …   Encyclopedia of vampire mythology

  • porphyria — n. any of a group of genetic disorders associated with abnormal metabolism of various pigments. Etymology: mod.L f. porphyrin purple substance excreted by porphyria patients f. Gk porphura purple …   Useful english dictionary

  • porphyria — noun Etymology: New Latin, from International Scientific Vocabulary porphyrin Date: 1923 any of several usually hereditary abnormalities of porphyrin metabolism characterized by excretion of excess porphyrins in the urine …   New Collegiate Dictionary

  • porphyria — Any of a group of disorders in which there is excessive excretion of porphyrins or their precursors …   Dictionary of molecular biology

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