31 research outputs found

    Infection By Cytomegalovirus In Patients With Neonatal Cholestasis

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    Background - Neonatal cholestasis syndrome with an intra or extrahepatic origin has been associated to viral infections. The participation of the cytomegalovirus in the etiopathogenesis of neonatal hepatitis has been already known for some time, but only recently there have been indications that this virus may be one of the possible etiological factors for extrahepatic biliary atresia. Aims - To assess the prevalence of infection by cytomegalovirus in patients with intrahepatic cholestasis and extrahepatic cholestasis. To compare the clinical characteristics of the intrahepatic cholestasis and extrahepatic cholestasis groups with the cytomegalovirus serological results. Patients and Methods - This study consisted of 76 patients with neonatal cholestasis who were admitted between January 1980 and January 1999 when they underwent a cytomegalovirus serologic study using the ELISA method. A case note was kept on each patient with the following data: age of patient at admission, serologic result for cytomegalovirus, history of maternal infection, prematurity, fetal distress, birth weight, ponderal gain, choluria and fecal acholia. The final anatomic diagnosis of cholestasis was based on the results of an abdominal ultrasonography, a liver biopsy and its evolution. The patients were then divided into two groups: group I - intrahepatic cholestasis and group II - extrahepatic cholestasis. Each of these groups were then divided into two subgroups: subgroup A - positive serology (IgM) for cytomegalovirus and subgroup B - negative serology (IgM) for cytomegalovirus. Results - The frequency of positive serology (IgM) for cytomegalovirus was 29.4% in children with intrahepatic cholestasis and 28.5% in children with extrahepatic cholestasis. In comparison with group IIB, group IIA presented a higher rate of maternal infection history. The patients in group IIA demonstrated a delayed access to the service in comparison with group IA. The groups did not demonstrate any significant differences regarding the onset age of jaundice, choluria and fecal acholia, birth weight and ponderal gain. Conclusions - The positive (IgM) seroprevalence for cytomegalovirus in children with intrahepatic cholestasis and extrahepatic cholestasis is high. The history of maternal infection was more common in extrahepatic cholestasis patients with positive serology for cytomegalovirus. There was a delay in the referral of these patients which resulted in a late diagnosis and surgical treatment.392132136Balistreri, W.F., Grand, R., Hoofnagle, J.H., Suchy, F.J., Ryckman, F.C., Perlmutter, D.H., Sokol, R.J., Biliary atresia: Current concepts and research directions (1996) Hepatology, 23, pp. 1682-1692Boppana, S.B., Pass, R.F., Britt, W.J., Stagno, S., Alford, C.A., Symptomatic congenital cytomegalovirus infection: Neonatal morbidity and mortality (1992) Pediatr Infect Dis J, 11, pp. 93-99Chang, M.H., Huang, H.H., Huang, E.S., Kao, C.L., Hsu, H.Y., Lee, C.Y., Polymerase chain reaction to detect human cytomegalovirus in livers of infants with neonatal hepatitis (1992) Gastroenterology, 103, pp. 1022-1025Fischler, B., Ehrnst, A., Forsgren, M., Örvell, C., Nemeth, A., The viral association of neonatal cholestasis in Sweden: A possible link between cytomegalovirus infection and extrahepatic biliary atresia (1998) J Pediatr Gastroenterol Nutr, 27, pp. 57-64Fowler, K.B., Stagno, S., Pass, R.F., Maternal age and congenital cytomegalovirus infection: Screening of two diverse newborn populations, 1980-1990 (1993) J Infect Dis, 168, pp. 552-556Griffiths, P.D., Baboonian, C., A prospective study of primary cytomegalovirus infection during pregnancy: Final report (1984) Br J Obstet Gynaecol, 91, pp. 307-315Hanshaw, J.B., Congenital cytomegalovirus infection: A fifteen year perspective (1971) J Infect Dis, 123, pp. 555-561Jevon, G.P., Dimmick, J.E., Biliary atresia and cytomegalovirus infection: A DNA study (1999) Pediatr Dev Pathol, 2, pp. 11-14Kumar, M.L., Nankervis, G.A., Cooper, A.R., Gold, E., Postnatally acquired cytomegalovirus infections in infants of CMV excreting mothers (1984) J Pediatr, 104, pp. 669-673Leinikki, P., Granstrüm, M.L., Santavuori, P., Pettay, O., Epidemiology of cytomegalovirus infections during pregnancy and infancy: A prospective study (1978) Scand J Infect Dis, 10, pp. 165-171Leinikki, P., Heinonen, K., Pettay, O., Incidence of cytomegalovirus infections in early childhood (1972) Scand J Infect Dis, 4, pp. 1-5Levinsohn, E.M., Foy, H.M., Kenny, G.E., Wentworth, B.B., Grayston, J.T., Isolation of cytomegalovirus from a cohort of 100 infant throughout the first year of life (1969) Proc Soc Exp Biol Med, 132, pp. 957-962Machado, C.M., Fink, M.C.D.S., Vilas Boas, L.S., Sumita, L.M., Weinberg, A., Shiguematsu, K., Souza, I.C., Pannuti, C.S., Infecção perinatal pelo citomegalovirus em hospital público do municipio de São Paulo: Estudo prospectivo (1991) Rev Inst Med Trop São Paulo, 33, pp. 159-166Mediaris, D.N., Observations concerning human cytomegalovirus infection and disease (1964) Bull Johns Hopkins, 114, pp. 181-211Nankervis, G.A., Kumar, M.L., Cox, F.E., Gold, E., A prospective study of maternal cytomegalovirus infection and its effect on the fetus (1984) Am J Obstet Gynecol, 149, pp. 435-440Poley, J.R., Syndromes of neonatal cholestasis (1993) Pediatric Gastroenterology and Hepatology. 3. 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São Paulo: McGraw-HillStagno, S., Pass, R.F., Dworsky, M.E., Henderson, R.E., Moore, E.G., Walton, P.D., Alford, C.A., Congenital cytomegalovirus infection: The relative importance of primary and recurrent maternal infection (1982) N Engl J Med, 306, pp. 945-949Stagno, S., Pass, R.F., Thomas, J.P., Navia, J.M., Dworsky, M.E., Defects of tooth structure in congenital cytomegalovirus infection (1982) Pediatrics, 69, pp. 646-648Stagno, S., Reynolds, D.W., Huang, E.S., Thames, S.D., Smith, R.J., Alford, C.A., Congenital cytomegalovirus infection: Occurrence in immune population (1977) N Engl J Med, 296, pp. 1254-1258Starr, J.G., Bart, R.D., Gold, E., Inapparent congenital cytomegalovirus infection: Clinical and epidemiologic characteristics in early infancy (1970) N Engl J Med, 282, pp. 1075-1078Tarr, P.I., Haas, J.E., Christie, D.L., Biliary atresia, cytomegalovirus and age at referral (1996) Pediatrics, 97, pp. 828-831Yamamoto, A.Y., Figueiredo, L.T.M., Mussi-Pinhata, M.M., Infecção perinatal por citomegalovirus: Muito freqüente mas pouco diagnosticada (1999) J Pediatr (Rio de Janeiro), 75, pp. 126-130Yamamoto, A.Y., Mussi-Pinhata, M.M., Pinto, P.C., Figueiredo, L.T., Jorge, S.M., Congenital cytomegalovirus infection in preterm and full-term newborn infants from a population with a high seroprevalence rate (2001) Pediatr Infect Dis J, 20, pp. 188-19

    Characterization of bovine respiratory syncytial virus isolated in Brazil

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    This paper presents the first isolation of bovine respiratory syncytial virus in Brazil and its physicochemical, morphological and molecular characterization. The virus was isolated from 33 samples of nasotracheal secretions, successively inoculated into a Madin-Darby bovine kidney cell culture, which was characterized by physicochemical tests and morphological observation by electron microscopy. The Brazilian sample is an RNA pleomorphic, enveloped, thermolabile and non-hemagglutinating spicular virus. Reverse transcription, followed by nested polymerase chain reaction (nRT-PCR) assay was carried out using oligonucleotides B1, B2A, B3 and B4 for the fusion proteins (F) and B5A, B6A, B7A and B8 for the attachment protein (G). The nRT-PCR-F amplified a fragment of 481 bp corresponding to part of the gene that codes for protein F, whereas nRT-PCR-G amplified a fragment of 371 bp, in agreement with part of the G gene. The virus isolated from Brazilian samples in this study corresponded to the bovine respiratory syncytial virus, and RT-PCR proved to be useful for the diagnosis of bovine clinical samples.21321

    Allan Sandage and the Cosmic Expansion

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    This is an account of Allan Sandage's work on (1) The character of the expansion field. For many years he has been the strongest defender of an expanding Universe. He later explained the CMB dipole by a local velocity of 220 +/- 50 km/s toward the Virgo cluster and by a bulk motion of the Local supercluster (extending out to ~3500 km/s) of 450-500 km/s toward an apex at l=275, b=12. Allowing for these streaming velocities he found linear expansion to hold down to local scales (~300 km/s). (2) The calibration of the Hubble constant. Probing different methods he finally adopted - from Cepheid-calibrated SNe Ia and from independent RR Lyr-calibrated TRGBs - H_0 = 62.3 +/- 1.3 +/- 5.0 km/s/Mpc.Comment: 12 pages, 11 figures, 1 table, Submitted to Astrophysics and Space Science, Special Issue on the Fundamental Cosmic Distance Scale in the Gaia Er

    Plantas medicinais de um remascente de Floresta Ombrófila Mista Altomontana, Urupema, Santa Catarina, Brasil

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