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Öğe Bilateral split feet: A new finding in Cornelia de Lange Syndrome(2010) Dogan D.G.; Dogan M.; Aslan M.; Karabiber H.We report on a male infant with Cornelia de Lange syndrome and bilateral split feet. Bilateral split feet do not appear to have ever been a reported feature in any of the published cases of Cornelia de Lange syndrome.Öğe Clinical features of children with henoch-schonlein: Purpura risk factors associated with renal involvement(2012) Tabel Y.; Inanc F.C.; Dogan D.G.; Elmas A.T.Introduction. This study aimed to evaluate renal involvement and factors affecting the prognosis in patients with Henoch-Schonlein purpura (HSP). Materials and Methods. The outcomes of 107 children diagnosed with HSP who had been followed up for at least 6 months were reviewed. Results. Renal involvement was observed in 26.1% of the patients. The mean age of the patients with renal involvement was 8.8±4.0 years as compared to 7.1±2.9 years in the patients without renal involvement (P=.02). The risk of renal involvement was found to be significantly higher in the patients who were 10 years old and over (P<.001). In the group with renal involvement, the frequency of scrotal involvement was significantly higher than that of the group without renal involvement (P=.02). The mean serum immunoglobulin A level of the patients with renal involvements was significantly higher (P=.04) and the mean serum complement C3 levels was significantly lower (P=.04) than those of the patients without renal involvement. None of the patients with renal involvement reached end-stage kidney failure. No significant relationship was observed between the development of renal involvement and early steroid treatment. Conclusions. This study proposes that in old children with HSP, elevated serum immunoglobulin A levels, decreased serum complement C3 levels, and scrotal involvement are associated with renal involvement. We failed to find any effect of steroid treatment on development of renal involvement.Öğe A Collodion baby with hypothyroidism(2010) Dogan D.G.; Aslan M.; Karabiber H.Collodion baby is a rare keratinizing congenital disorder. Although it is milder in degree than harlequin fetus, the infant is at risk for increased water loss, thermal instability, percutaneous toxicity, and infection as a result of an impaired skin barrier function. Here we report on an 11 days-old collodion baby with hypernatremic dehydratation, septicemia and congenital hypothyroidism. To our knowledge congenital hypothyroidism associated with collodion baby is reported in only one case up to date.Öğe Hallermann-Streiff syndrome with hemihypertrophy(2010) Dogan D.G.; Karabiber H.; Erhan M.D.; Garipardic M.; Davutoglu M.; Guler E.We report on a five year old girl with Hallermann-Streiff syndrome and hemihypertrophy. Hemihypertrophy does not appear to have ever been associated with Hallermann-Streiff syndrome.Öğe In reference to Improved outcomes after low-concentration hypochlorous acid nasal irrigation in pediatric chronic sinusitis(John Wiley and Sons Inc., 2016) Dogan D.G.; Dogan M.[No abstract available]