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1.
Int J Tuberc Lung Dis ; 14(7): 916-20, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20550778

RESUMO

SETTING: Tuberculous rheumatism (Poncet's disease) is a reactive polyarthropathy associated with extra-pulmonary and pulmonary tuberculosis (TB) without evidence of mycobacterial infection of the involved joints. As all patients with TB do not present with this peculiar clinical feature, a genetic susceptibility is suspected. OBJECTIVE: To determine the major histocompatibility complex (MHC) class I and II alleles in Mexican mestizo patients with Poncet's disease. DESIGN: In this case-control study of 16 Mexican mestizo patients diagnosed with Poncet's disease and 99 ethnically matched healthy controls, high resolution human leukocyte antigen (HLA) typing was performed for HLA-A, B, DR and DQ by polymerase chain reaction. HLA-DRB1 and HLA-DQB1 subtypes were performed by sequence-specific oligonucleotide probe hybridization. RESULTS: A significantly increased frequency of HLA-B27 (corrected P = 0.01) and DQB1*0301 (corrected P = 0.0009) alleles and decreased frequency of HLA-DQB1*0302 (corrected P = 0.00001) were identified in patients compared to healthy controls. CONCLUSION: These data suggest that genes located within the MHC may play a role in the susceptibility to Poncet's disease in patients diagnosed with TB.


Assuntos
Predisposição Genética para Doença , Antígenos HLA/genética , Tuberculose Osteoarticular/genética , Adulto , Alelos , Estudos de Casos e Controles , Feminino , Genes MHC Classe I/genética , Genes MHC da Classe II/genética , Antígeno HLA-B27/genética , Antígenos HLA-DQ/genética , Cadeias beta de HLA-DQ , Humanos , Masculino , México , Pessoa de Meia-Idade , Sondas de Oligonucleotídeos , Reação em Cadeia da Polimerase , Adulto Jovem
2.
Ginecol Obstet Mex ; 63: 163-5, 1995 Apr.
Artigo em Espanhol | MEDLINE | ID: mdl-7768473

RESUMO

Pituitary adenoma, familiar type, with apparent affection over the involved somatomammotropin of secretion of growth hormone and prolactin, with dominant autosomic transmission, is described for the first time. It was seen that a couple of members without demonstrable tumour, showed clinical data (phenotype) of acromegaly. On investigation of histocompatibility antigens it was observed that the patients with tumour and other symptomatic ones, but without tumour, shared the same haplotypes, and so is very possible that investigation of HLA antigens in patients with pituitary tumour, contributes to better identify its nature and frequency.


Assuntos
Acromegalia/genética , Adenoma/genética , Neoplasias Hipofisárias/genética , Acromegalia/complicações , Adenoma/complicações , Adulto , Feminino , Antígenos HLA/análise , Haplótipos , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Neoplasias Hipofisárias/complicações
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