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1.
Nepal Med Coll J ; 14(1): 1-4, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23441485

RESUMO

The vanishing testis with maleness is a rare syndrome with frequency of 1 in 20,000 males. Here, we report about a 30 years old male subject with vanishing testis syndrome, feminization and gynecomastia. Follicle stimulating hormone (FSH) and Leutinizing hormone (LH) levels were elevated whereas testosterone was below normal and anti-mullerian-hormone level was undetectable in the patient. The chromosomal analysis and DNA analysis of SRY and ZFY, DAX-I, AZFa, AZFb, AZFc and heterochromatic region of Y chromosome with STS primer (sY160) were done to detect any genetic changes at specified sites (both at chromosomal and molecular level). Karyotyping confirmed patient as 46, XY male, with no evidence of mosaicism in blood cells. PCR amplification of SRY gene indicated that the SRY gene of the patient was normal. PCR amplification of SRY, ZFY, DAX-I, AZFa, AZFb, AZFc gene and Y chromosome heterochromatic region using STS primer sY(160) did not reveal any microdeletions. The anti-mullerian-hormone level was undetectable indicating that the patient didn't have any testicular tissue in scrotum. Increased levels of FSH, LH and reversed androgen: estrogen ratio might have given rise to gynecomastia in the patient. SRY-positive 46,XY male with vanishing testis might be due to torsion of testis during descent in fetal period. The torsion of testis might have caused vascular occlusion and thereby regression of testicular tissue occurred, but the exact genetic condition yet to understand.


Assuntos
Feminização/genética , Genes sry , Disgenesia Gonadal 46 XY/genética , Ginecomastia/genética , Adulto , Hormônio Antimülleriano/sangue , Diagnóstico por Imagem , Feminização/diagnóstico , Hormônio Foliculoestimulante/sangue , Disgenesia Gonadal 46 XY/diagnóstico , Ginecomastia/diagnóstico , Humanos , Cariotipagem , Hormônio Luteinizante/sangue , Masculino , Reação em Cadeia da Polimerase , Síndrome , Testículo/anormalidades , Testosterona/sangue
2.
Nepal Med Coll J ; 11(3): 147-51, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20334059

RESUMO

Ciprofloxacin is a bactericidal drug which is being used widely throughout the world for the treatment of various bacterial infection. Cytotoxicity and genotoxicity of Ciprofloxacin on human lymphocytes in vitro had been assessed taking various parameters like mitotic index (MI), chromosome aberration (CA), anaphase anomalies, replicative index (RI) and sister chromatid exchange (SCE) as end points. Our results indicate low mitotic index, low replicative index and high frequency of anaphase anomalies on one hand and on other hand, high frequency of chromosome aberration and sister chromatid exchanges (SCEs) in the exposed groups as compared to that of control group. These are the indications of both cytotoxicity and genotoxicity of Ciprofloxacin on human lymphocyte culture in vitro. All the parameters obtained from the experimental group were statistically significant when compared to that of control.


Assuntos
Anti-Infecciosos/uso terapêutico , Ciprofloxacina/uso terapêutico , Linfócitos/efeitos dos fármacos , Adulto , Aberrações Cromossômicas/efeitos dos fármacos , Humanos , Técnicas In Vitro , Masculino , Índice Mitótico , Troca de Cromátide Irmã/efeitos dos fármacos , Adulto Jovem
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