Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Añadir filtros








Intervalo de año
1.
Indian Pediatr ; 2012 April; 49(4): 311-313
Artículo en Inglés | IMSEAR | ID: sea-169298

RESUMEN

We examined for osteopontin (OPN) gene C/T polymorphism in 78 patients (53 girls) with vesicoureteric reflux, with or without renal scarring. The T allele frequency was associated with a significantly increased risk (26.4 fold) of renal scarring.

2.
Indian J Pediatr ; 2008 Jun; 75(6): 632-4
Artículo en Inglés | IMSEAR | ID: sea-81513

RESUMEN

An offspring of marriage between two first cousins presented with atonic seizures developed on the 20(th) day of life. The physical examination of the case was normal. In laboratory results, Ca(+2) level was 5.7 mg/dl, Mg(+2): 0.4 mg/dl (1,3-2,1), PTH: 28.4 pg/ml (12-92), and P-: 4.5 mg/dl. The case was diagnosed as hypomagnesemia with secondary hypocalcemia (HSH) and TRPM6 gene mutation analysis revealed a homozygote mutation of E157X.


Asunto(s)
Calcio/metabolismo , Análisis Mutacional de ADN , Humanos , Hipocalcemia/etiología , Lactante , Magnesio/metabolismo , Deficiencia de Magnesio/complicaciones , Masculino , Linaje , Convulsiones , Análisis de Secuencia de ADN , Canales Catiónicos TRPM/genética
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA