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1.
J Pediatr ; 139(2): 204-9, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11487744

RESUMO

OBJECTIVE: To search for mutations in melanocortin pathway elements, that is, the melanocortin-4 receptor (MC4R ), agouti-related protein (AGRP ), and (alpha-melanocyte-stimulating hormone (alpha MSH ) genes in children with severe obesity. STUDY DESIGN: Direct sequencing of the MC4R encoding sequence and single-strand polymorphism conformation analysis of AGRP and alpha MSH genes were performed in 63 severely obese children. Polymerase chain reaction (PCR) assays of restriction fragment length polymorphism were used to assess the frequency of each newly discovered mutation in 283 non-obese control subjects. RESULTS: Four dominantly inherited, heterozygous, missense MC4R mutations (Val50Met, Ser58Cys, Ile102Ser, and Ile170Val) were identified in 4 unrelated children and none of the control subjects. Expression of the obese phenotype was variable in mutation-positive family members. Clinical and laboratory features were similar in the obese children with and without an MC4R mutation. Two polymorphisms were detected in the AGRP -encoding sequence (a silent mutation in exon 1 and Ala67Thr in exon 2), with similar frequencies in the obese and control groups. No mutations were found in the alpha MSH gene. CONCLUSIONS: MC4R mutations may be a non-negligible cause of severe obesity in children with variable expression and penetrance. Mutations in AGRP and alpha MSH genes were not among the causes of obesity in our population.


Assuntos
Análise Mutacional de DNA , Hormônios Estimuladores de Melanócitos/genética , Obesidade/genética , Proteínas/genética , Receptores de Peptídeos/genética , Adolescente , Proteína Relacionada com Agouti , Índice de Massa Corporal , Estudos de Casos e Controles , Criança , Pré-Escolar , Feminino , Humanos , Peptídeos e Proteínas de Sinalização Intercelular , Masculino , Linhagem , Reação em Cadeia da Polimerase , Polimorfismo Genético , Polimorfismo de Fragmento de Restrição , Receptor Tipo 4 de Melanocortina
4.
Am J Clin Pathol ; 100(2): 99-102, 1993 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-8356956

RESUMO

The present study was developed to verify whether a reduction in phospholipid concentration could increase the activated partial thromboplastin time (APTT) sensitivity to detect lupus anticoagulant (LA) during pregnancy. The authors studied 38 pregnant women (10 normal subjects and 28 patients with associated clinical complications) and 40 nonpregnant control subjects. Tests to detect LA, including APTT, platelet neutralization procedure (standard APTT), the kaolin clotting time, the diluted Russell viper venom test neutralized by lysed platelets, and factor assays, were performed. Positive results were found in 5 of 28 pregnant women with associated clinical complications. The APTT, using three different phospholipid concentrations (standard and more diluted cephalin), was performed on plasma samples and on its 1:1 mixture with normal plasma. The behavior of standard and diluted APTT was similar in negative LA pregnant women and nonpregnant control subjects. The mean values showed nonsignificant differences. Four of five pregnant women with positive LA findings had a prolonged APTT, which was not corrected by the addition of normal plasma using standard conditions. When diluted phospholipids were used, only one of them had a prolonged APTT that was corrected by the addition of normal plasma. Therefore, the highest sensitivity (80%) and specificity (100%) of the APTT to detect LA in pregnant women were obtained using the standard conditions.


Assuntos
Inibidor de Coagulação do Lúpus/análise , Tempo de Tromboplastina Parcial , Gravidez/sangue , Feminino , Humanos , Concentração Osmolar , Fosfolipídeos/sangue , Complicações na Gravidez/sangue , Valores de Referência , Sensibilidade e Especificidade
5.
Am J Hematol ; 35(3): 208-9, 1990 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-2220766

RESUMO

A boy with umbilical bleeding and severe hemorrhages after minor trauma, without family bleeding history, was studied. Coagulation tests showed abnormalities in FXIII subunits and FVIII/vWF complex. Both parents presented results compatible with a heterozygote state for FXIII deficiency and the father had abnormalities of FVIII/vWF. The propositus was diagnosed as congenital FXIII deficiency associated with vWD. No severe hemorrhagic complication was observed after a prophylactic regimen with cryoprecipitates.


Assuntos
Deficiência do Fator XIII/complicações , Doenças de von Willebrand/complicações , Deficiência do Fator XIII/sangue , Deficiência do Fator XIII/diagnóstico , Feminino , Humanos , Lactente , Masculino , Doenças de von Willebrand/sangue , Doenças de von Willebrand/diagnóstico
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