DEFICIENCIA DE G6PD PDF

6 dez. O estudo compreendeu a avaliação da deficiência de GlicoseFosfato Desidrogenase (G6PD) e perfil hematológico em indivíduos ( Glucosephosphatase dehydrogenase (G6PD) deficiency is the most common enzyme deficiency in humans, affecting million people. La deficiència de G6PD està estretament relacionada amb el favisme, un trastorn que es caracteritza per una reacció hemolítica al consum de faves. El nom de.

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The other 3 variants were accompanied by very severe G6PD deficiency.

Katsuragawa I ; Dd H. In Brazil and other LA countries facing malaria as a public health problem, the treatment recommendation for P. G6PDd among Amerindian populations – This systematic review analysed 24 publications regarding G6PDd prevalence among Amerindians belonging to 55 ethnic groups living in 12 countries and 64 different villages.

Nonspherocytic congenital hemolytic anemia due to a new GPD variant: Hereditary hemolytic anemia associated with glucosephosphate dehydrogenase deficiency Mediterranean type.

See Beutler et al. Both had had normal G6PD biochemical screening tests.

Deficiència de glucosafosfat-deshidrogenasa – Viquipèdia, l’enciclopèdia lliure

The G6PD Gifu variant was discovered in a 9-year-old Japanese male with chronic hemolysis and hemolytic crises after upper respiratory infections Fujii et al. The mutation created an Fnu4HI restriction site, which was used to confirm the mutation.

See Gaetani et al. A new variant of human erythrocyte glucosephosphate dehydrogenase: Glucosephosphate dehydrogenase deficiency deficinecia a native Danish family: A novel RH mutation in the glucosephosphate dehydrogenase gene in the tribal groups of the Nilgiris in southern India.

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Incidence evaluation of GlucosePhosphate Dehydrogenase and hematological profile in Rondonia

Glucosephosphate dehydrogenase G6PD mutations database: See Yermakov et al. See Mentzer et al. In parallel with the virtual absence of G6PDd among Amerindian populations, the literature indicates that these groups of people are not susceptible to haemolysis caused by oxidative stressors such as PQ and other drugs. In a US white patient with nonspherocytic hemolytic anemiaBeutler et al. Linkage between the X chromosome loci for glucosephosphate dehydrogenase electrophoretic variation and hemophilia A.

See Fujii et al. By comparable methods, Hors-Cayla et al.

Spatial distribution of G6PD deficiency variants across malaria-endemic regions. Scriver CR et al. Glucosephosphate dehydrogenase Buenos Aires: Most of the countries presenting cases of PQ-induced haemolysis present a higher prevalence of G6PDd when compared to other countries.

This aberrant G6PD associated with nonspherocytic hemolytic anemia was veficiencia by Elizondo et al. This scarcity of data constitutes a major limitation for a more reliable understanding of G6PDd epidemiology in LA.

See Usanga et al. Studies on several genetic hematological traits of the Mexican population. See Sidi et al. A statistically significant relationship was found in the activity of G6PD in erythrocytes and xeficiencia of male subjects.

Effects of immigration on the prevalence of malaria in rural areas of the Amazon Basin of Brazil. G6PD activity was undetectable not only in the patient’s red blood cells but also in leukocytes defciiencia fibroblasts, and an immunologically crossreacting material was undetectable in these tissues.

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G6PD deficiency in Latin America: systematic review on prevalence and variants

Rapid tests have the potential to change radically the healthcare process for patients presenting G6PDd, potentially also allowing the optimisation of available financial resources because deficiency diagnosis likely decreases other costs such as those related to hospitalisations.

See Vaca et al.

A map of amino acids showing the location of mutations, including double mutations, was provided. They suggested G6PD Santiago as the designation. There is a G6PD Mexico; see under Mem Inst Oswaldo Cruz ;84 4: Glucosephosphate dehydrogenase GPD mutations in Mexico: See Krasnopolskaya et al. Reliable exclusion of patients at risk of severe harm opens the possibility for safer and more effective deployment of high dose regimens.

Surprisingly, the enzyme appeared to the authors to be more stable than normal G6PD, whereas most deficient variants have lowered stability. Substitution eeficiencia adenine for guanine at nucleotide leads to substitution of alanine by threonine at amino acid position Vulliamy et al.

Deficiència de glucosa-6-fosfat-deshidrogenasa

By study of cell hybrids, Shows et al. See Nakai and Yoshida See Castro and Snyder Rev Cubana Hematol Inmunol Hemoter. A variant glucosephosphate dehydrogenase Gd – Chiapas associated with moderate enzyme deficiency and occasional hemolytic anemia.