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1.
Arch Razi Inst ; 78(4): 1225-1237, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-38226382

RESUMO

Heavy metals are among the most important environmental pollutants which accumulate in various organs and are associated with several toxic effects. This study was performed to determine the status of heavy metals in river buffaloes in Khuzestan province, Iran, and its relationship with hematologic and serum biochemical parameters. A total of 103 apparently healthy buffaloes were sampled from the region. The concentration of heavy metals, including lead (Pb), mercury (Hg), and cadmium (Cd), was determined in serum samples by atomic spectroscopy. In addition, complete blood counts and serum biochemical profiles were assessed. The serum concentration of Cd, Pb, and Hg in the sampled buffaloes, as mean±standard error, were 0.55±0.01, 6.51±0.10, and 6.28±0.09 µg/l, respectively, which are within the permissible serum levels in the livestock. Serum Cd and Hg levels showed no significant relationship with hematologic or biochemical analytes. However, there were significant negative correlations between Pb levels and phosphorus, magnesium, sodium, as well as potassium concentrations, while serum iron was positively correlated with lead (P<0.05). In addition, there was a significant positive correlation between Hg level and serum aspartate aminotransferase activity (P<0.05). Despite the fact that river buffaloes in Khuzestan spend a long time daily in the Karun River with high industrial pollution, no serum evidence of heavy metal toxicity was found in these animals. It can be suggested that river buffaloes in Khuzestan seem to be resistant to the environmental pollution caused by heavy metals. However, further studies are required to confirm this issue and identify its possible explanations.


Assuntos
Mercúrio , Metais Pesados , Animais , Cádmio/análise , Búfalos , Irã (Geográfico)/epidemiologia , Rios/química , Chumbo , Metais Pesados/análise , Mercúrio/análise
2.
Cancer Genet Cytogenet ; 69(2): 153-5, 1993 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-8402556

RESUMO

Cytogenetic analysis provides valuable prognostic information in children diagnosed with hematologic malignancies. While the t(4;11)(q21;q23) has frequently been reported in patients with acute lymphoblastic leukemia, the additional involvement of chromosome 13 to form a three-way translocation has not been described previously. We report a case of acute lymphoblastic leukemia in a 5-month old infant with a complex t(4;11;13)(q21;q23;q12-14).


Assuntos
Linfoma de Burkitt/genética , Cromossomos Humanos Par 11 , Cromossomos Humanos Par 13 , Cromossomos Humanos Par 4 , Leucemia-Linfoma Linfoblástico de Células Precursoras B/genética , Translocação Genética , Linfoma de Burkitt/diagnóstico , Linfoma de Burkitt/imunologia , Feminino , Humanos , Imunofenotipagem , Lactente , Cariotipagem , Leucemia-Linfoma Linfoblástico de Células Precursoras B/diagnóstico , Leucemia-Linfoma Linfoblástico de Células Precursoras B/imunologia
3.
Ann Genet ; 34(3-4): 252-5, 1991.
Artigo em Inglês | MEDLINE | ID: mdl-1809235

RESUMO

A 15.5-year-old female was referred for primary amenorrhea and slow development of secondary sex characteristics. The karyotype revealed 45,X/46,X,+mar (75%/25%). The small marker chromosome was C-band and Q-band negative. It appeared to be primarily centromeric with some light G-band staining material on either side. Females with Y-chromosomal material are at an increased risk for gonadal neoplasia and this patient was studied further to investigate the possibility that the marker was a deleted Y chromosome. Polymerase chain reaction (PCR) analysis of this patient's DNA revealed the presence of Y-chromosomal material presumably derived from the marker chromosome. These results indicate that the PCR technique, in conjunction with cytogenetic analysis, can identify possible Y-chromosomal material. This testing provides critical information necessary for correct medical followup of Turner syndrome mosaic patients.


Assuntos
DNA/análise , Mosaicismo/genética , Síndrome de Turner/genética , Cromossomo Y , Adolescente , Feminino , Marcadores Genéticos/genética , Humanos , Cariotipagem , Reação em Cadeia da Polimerase , Aberrações dos Cromossomos Sexuais/genética
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