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Abstract:

The porphyrias are a group of inherited metabolic disorders of heme biosynthesis which result from a partial deficiency in one of its seven specific enzymes, after its first and rate limiting enzyme, delta-aminolevulinic acid synthetase. They can be classified on the basis of their clinical manifestations into cutaneous, acute and mixed disorders. Acute intermittent porphyria (AIP) is the most common type of hepatic acute porphyrias, inherited as an autosomal dominant trait, caused by a defect in the gene which codifies for the heme enzyme porphobilinogen deaminase. Its prevalence in the Argentinean population is about 1:125,000. A partial deficiency in another enzyme, protoporphyrinogen oxidase, produces variegate porphyria (VP), the second acute porphyria most frequent in the Argentinean population (1:600,000). Here, we review all the mutations we have found in 46 AIP and 9 VP unrelated Argentinean patients. To screen for mutations in symptomatic patients, we have proposed a geneticresearch strategy.

Registro:

Documento: Artículo
Título:Acute porphyrias in the Argentinean population: a review.
Autor:Parera, V.E.; De Siervi, A.; Varela, L.; Rossetti, M.V.; Batlle, A.M.
Filiación:Centro de Investigaciones sobre Porfirinas y Porfirias, CONICET and Fac. Ciencias Exactas y Naturales, University of Buenos Aires, Argentina
Palabras clave:acute intermittent porphyria; Argentina; genetics; hepatic porphyria; human; metabolism; mutation; review; Argentina; Humans; Mutation; Porphyria, Acute Intermittent; Porphyrias, Hepatic
Año:2003
Volumen:49
Número:4
Página de inicio:493
Página de fin:500
Título revista:Cellular and molecular biology (Noisy-le-Grand, France)
Título revista abreviado:Cell. Mol. Biol. (Noisy-le-grand)
ISSN:01455680
PDF:https://bibliotecadigital.exactas.uba.ar/download/paper/paper_01455680_v49_n4_p493_Parera.pdf
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01455680_v49_n4_p493_Parera

Citas:

---------- APA ----------
Parera, V.E., De Siervi, A., Varela, L., Rossetti, M.V. & Batlle, A.M. (2003) . Acute porphyrias in the Argentinean population: a review. Cellular and molecular biology (Noisy-le-Grand, France), 49(4), 493-500.
Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01455680_v49_n4_p493_Parera [ ]
---------- CHICAGO ----------
Parera, V.E., De Siervi, A., Varela, L., Rossetti, M.V., Batlle, A.M. "Acute porphyrias in the Argentinean population: a review." Cellular and molecular biology (Noisy-le-Grand, France) 49, no. 4 (2003) : 493-500.
Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01455680_v49_n4_p493_Parera [ ]
---------- MLA ----------
Parera, V.E., De Siervi, A., Varela, L., Rossetti, M.V., Batlle, A.M. "Acute porphyrias in the Argentinean population: a review." Cellular and molecular biology (Noisy-le-Grand, France), vol. 49, no. 4, 2003, pp. 493-500.
Recuperado de https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01455680_v49_n4_p493_Parera [ ]
---------- VANCOUVER ----------
Parera, V.E., De Siervi, A., Varela, L., Rossetti, M.V., Batlle, A.M. Acute porphyrias in the Argentinean population: a review. Cell. Mol. Biol. (Noisy-le-grand). 2003;49(4):493-500.
Available from: https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01455680_v49_n4_p493_Parera [ ]