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1.
Chinese Journal of Integrated Traditional and Western Medicine ; (12): 931-933, 2008.
Artículo en Chino | WPRIM | ID: wpr-360520

RESUMEN

<p><b>OBJECTIVE</b>To explore the clinical effects of colonic dripping with Taihuang liquid (THL) in treating neonatal hyperbilirubinemia (HBE).</p><p><b>METHODS</b>One hundred and thirty-eight neonates with HBE were randomly assigned to two groups. Conventional treatment and nursing were given to both groups, and THL was given additionally to the observation group by colonic dripping.</p><p><b>RESULTS</b>Significant differences between the observation group and the control group were shown in frequency of defecation (4.6 +/- 1.3 times/d vs 2.0 +/- 1.1 times/d), daily serum bilirubin reduction (31.5 +/- 10.1 micromol/L vs 23.3 +/- 8.3 micromol/L), and days for normalizing serum bilirubin level (5.6 +/- 3.5 d vs 7.8 +/- 4.1 d, all P < 0.01).</p><p><b>CONCLUSION</b>Colonic dripping of THL could promote the excretion of bilirubin, so as to decrease the level of serum bilirubin in neonates with HBE.</p>


Asunto(s)
Femenino , Humanos , Lactante , Recién Nacido , Masculino , Bilirrubina , Sangre , Medicamentos Herbarios Chinos , Hiperbilirrubinemia Neonatal , Sangre , Quimioterapia
2.
Chinese Medical Journal ; (24): 1418-1421, 2004.
Artículo en Inglés | WPRIM | ID: wpr-291909

RESUMEN

<p><b>BACKGROUND</b>Corneal dystrophy is a group of inherited blinding diseases of the cornea. This study was to identify the mutations of the keratoepithelin (KE) gene for proper diagnosis of corneal dystrophy.</p><p><b>METHODS</b>Three families with corneal dystrophy were analysed. Thirteen individuals at risk for corneal dystrophy in family A, the proband and her son in family B, and the proband in family C were examined after their blood samples were obtained. Mutation screening of human transforming growth factor beta-induced gene (BIGH3 gene) was performed.</p><p><b>RESULTS</b>Five individuals in family A were found by clinical evaluation to be affected with granular corneal dystrophy and carried the BIGH3 mutation W555R. However, both probands in families B and C, also diagnosed with granular corneal dystrophy, harboured the BIGH3 mutation R124H.</p><p><b>CONCLUSION</b>Molecular genetic analysis can improve accurate diagnosis of corneal dystrophy.</p>


Asunto(s)
Adolescente , Adulto , Niño , Preescolar , Femenino , Humanos , Masculino , Persona de Mediana Edad , Distrofias Hereditarias de la Córnea , Genética , Patología , Proteínas de la Matriz Extracelular , Genética , Mutación , Factor de Crecimiento Transformador beta , Genética
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