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1.
Clin Exp Immunol ; 49(2): 310-6, 1982 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-6982135

RESUMEN

The incidence of serum antinuclear antibodies and serum antibodies to single stranded (ss) and double stranded (ds) DNA was investigated following acute malaria in 58 Caucasians visiting tropical countries but resident in Britain and in 24 Ghanaians resident in Ghana. In Caucasians this infection was associated with a significant increase in the incidence of speckled antinuclear antibodies (38% compared to 3% in controls; P less than 0.001) and a significant rise in antibody levels against ssDNA (14% compared to 5%; P less than 0.05), but no rise in antibodies against dsDNA. Acute malaria in Ghanaians was associated with an incidence of 25% of antinuclear antibodies and 4% of antibodies to ssDNA; these were similar to those found in healthy Ghanaians who are chronically exposed to malaria. Antibodies against dsDNA were not detected. The incidence of antinuclear antibodies and levels of anti-ssDNA antibodies was higher in the Ghanaian healthy population than in normal Caucasians. These observations indicate that malaria is associated with the development of antinuclear and anti-ssDNA antibodies. Ghanaian patients with a tropical splenomegaly syndrome or with a nephrotic syndrome, both of which conditions are suspected of having a malarial aetiology, had serum levels of anti-ssDNA higher than healthy controls. This observation adds further circumstantial evidence to the role of malaria in causing anti-DNA antibodies.


Asunto(s)
Anticuerpos Antinucleares/análisis , ADN de Cadena Simple/inmunología , Malaria/inmunología , Adulto , ADN/inmunología , Humanos , Inmunoglobulina G/análisis , Síndrome Nefrótico/inmunología , Esplenomegalia/inmunología
2.
Trop Geogr Med ; 29(3): 237-44, 1977 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-595129

RESUMEN

Early in 1973 residents of 20 randomly selected rural villages in southern Ghana were studied to determine the prevalence of anaemia. Laboratory tests were conducted to learn what haemoglobin phenotypes were present and the distribution of white blood cell counts. Moderate anaemia (below 10 g%) was fairly common, particularly in children and 15--29 year old women, but severe anaemia (below 7 g%) was rare. Malaria infection and diets with low iron content were major factors affecting haemoglobin level, while hookworm infestation and high parity had little effect. Neutropenia (about two-thirds of Caucasian values) and the distribution of haemoglobin types (AS 16.3%; AC 11.1%) were similar to findings in earlier studies. To improve haemoglobin levels in children and young women, low-cost intervention programmes based on volunteer village workers are recommended.


Asunto(s)
Agranulocitosis/epidemiología , Anemia/epidemiología , Hemoglobinas/análisis , Neutropenia/epidemiología , Adolescente , Adulto , Factores de Edad , Niño , Preescolar , Eosinófilos , Femenino , Ghana , Infecciones por Uncinaria/epidemiología , Humanos , Recuento de Leucocitos , Linfocitos , Malaria/epidemiología , Masculino , Persona de Mediana Edad , Neutrófilos , Embarazo , Población Rural , Factores Sexuales , Bazo
3.
Pediatr Res ; 11(2): 147-52, 1977 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-840505

RESUMEN

Hematologic and globin chain synthesis studies have been made in 21 children, aged 2 to 6 years, many of their parents, and several normal adults and alpha-thalassemia heterozygotes. At birth, 11 children had about 5% hemoglobin (Hb) Bart's, 5 had about 2% Hb Bart's, and 5 had no trace of Hb Bart's. A significant decrease in mean corpuscular volume. (MCV) and mean corpuscular hemoglobin (MCH) values and an increase in the beta/alpha ratio was observed in the first group; microcytosis and hypochromia were absent in the children of the second group although the beta/alpha ratio was significantly increased. The alpha chain deficiency is familial. Increased alpha/alpha ratios were present in many parents although only two parents of children with 5% Hb Bart's at birth had hematologic findings suggestive of the presence of the same type of defect as observed in the children with the larger amount of Hb Bart's at birth.


Asunto(s)
Hemoglobinopatías/genética , Adulto , Población Negra , Niño , Preescolar , Eritrocitos/crecimiento & desarrollo , Femenino , Genotipo , Georgia , Hematócrito , Hemoglobinometría , Hemoglobinopatías/sangre , Hemoglobinas Anormales , Humanos , Recién Nacido , Estudios Longitudinales , Masculino , Linaje , Talasemia/genética
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