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

ABSTRACT

<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>


Subject(s)
Female , Humans , Infant , Infant, Newborn , Male , Bilirubin , Blood , Drugs, Chinese Herbal , Hyperbilirubinemia, Neonatal , Blood , Drug Therapy
2.
Chinese Medical Journal ; (24): 1418-1421, 2004.
Article in English | WPRIM | ID: wpr-291909

ABSTRACT

<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>


Subject(s)
Adolescent , Adult , Child , Child, Preschool , Female , Humans , Male , Middle Aged , Corneal Dystrophies, Hereditary , Genetics , Pathology , Extracellular Matrix Proteins , Genetics , Mutation , Transforming Growth Factor beta , Genetics
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