El síndrome de Gilbert es una enfermedad hepática frecuente e inofensiva en la cual el hígado no procesa la bilirrubina de manera adecuada. COLELITIASIS Y COLEDOCOLITIASIS Esp. Ana Maria Bastidas E. Bilirrubina directa (0,1 a 0,3 mg/ ml); Bilirrubina indirecta (menor de. Cuando existe hiperbilirrubinemia directa, dada la hidrosolubilidad de esta renal; por el contrario, la bilirrubina indirecta (BI) o no conjugada es liposoluble y su colestasis intensa e inyección conjuntival (leptospirosis icterohemorrágica).
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Universidad Nacional de Colombia. Se descartaron diversas causas de hiperbilirrubinemia directa en el neonato.
Jaundice is a commonly occurring problem in hospitals’ neonatal units. This report describes a newborn with hypefbilirrubinaemia; the clinical picture was initially dominated by the unconjugated bilirubin fraction and later by anaemia, hepatomegaly, increased conjugated bilirubin fraction, impaired liver function, renal tubular dysfunction, cataracts and injury to CNS white matter. Various causes of direct hyperbilirrubinaemia in the newborn were ruled out.
Thin-layer chromatography revealed urine-reducing substances i. A marked reduction in galactose uridyl transferaseactivity was documented, thereby confirming a diagnosis of galactosaemia. Breastfeedingwas discontinued and soy milk started which led to the symptoms becoming resolved. Glucosephosphate dehydrogenase and red cell pyruvate kinase deficiency in neonatal jaundice cases in egypt.
ICTERICIA vs PALIDEZ by martha isabel delgado cordoba on Prezi
J Pediatr Hematol Oncol. Ictericia e hipoglicemia neonatal: Early and severe indirect hyperbilirubinemia as a manifestation of galactosemia. Kwon C, Farrell PM. The magnitude and challenge of falsepositive newborn screening test results. Arch Pediatr Adolesc Med. Classical galactosaemia in Chinese: A case report and review of disease incidence. J Paediatr Child Health. Screening for galactosaemia in Greece.
Early diagnosis of inherited metabolic disorders towards improving outcome: Selective screening for neonatal galactosemia: Simultaneous occurrence of various mutations and polymorphisms in cis and in trans of the galactosephosphate uridyl-transferase gene in a Turkish family with classical galactosemia. J Mol Med Berl. The metabolic and molecular bases of inherited disease.
Mac Graw Hill Inc; Congenital galactosemia detected by severe Escherichia coli infections. Galactose inhibition of neonatal neutrophil function. Association of Fungal Sepsis and Galactosemia. Galactosemia with Chorea -An unusual presentation. Purpura fulminans in a newborn infant with galactosemia.
Revista de la Facultad de Medicina
Vitreous hemorrhage as an ophthalmic complication of galactosemia. When is it a newborn screening emergency? Proton MR spectroscopy and imaging of a galactosemic patient before and after dietary treatment. In vivo evidence of brain galactitol accumulation in an infant with galactosemia and encephalopathy. Prenatal diagnosis of galactosemia.
Diversity of approaches to classic galactosemia around the world: J Inherit Metab Dis. Longitudinal assessment of intellectual achievement in patients with classical galactosemia.
Inborn errors of metabolism in infancy: The clinical and molecular spectrum of galactosemia in patients from the Cape Town region of South Africa. Cornejo V, Raiman E.
Rev Chil Nutr [internet]. Clinical pictures of 75 patients with neonatal intrahepatic cholestasis caused by citrin deficiency NICCD. Hiperamonemia neonatal causada por defectos del ciclo de la urea. Dieecta Island metabolic newborn screening: A case report of argininosuccinic aciduria ASA. Med Health R I.
Publindex is a Colombian bibliographic index for classifying, updating, rating and certifying scientific and hiperbbilirrubinemia publications.
DOAJ increases the visibility and ease of use of open access scientific and scholarly journals, aims to be comprehensive and cover all that journals that use a quality control system to guarantee the content. It’s a one stop shop for users of OA Diretca. It is currently being managed in Colombia by the Universidad Nacional de Colombia.
Scopus is a bibliographic database publishing summaries and references concerning articles from scientific journals. Hiperbilirurbinemia covers around 19, titles by more than 5, international editors, including coverage of about 16, journals.
Latindex is the product of cooperation by a network of Latin-American institutions operating in a coordinated way to gather and disseminate bibliographic information about serialised scientific publications produced in the region.
Get a more complete global picture by discovering new insights from research in Latin America, Spain, Portugal, the Caribbean and South Africa. Search and view critically important regional content with international impact to get a comprehensive picture of the influencers and drivers of regional research. Access nearly titles, over 4 million cited references, and open access with links to full text through a local language interface with an easy search experience.
Galactosemia como causa de ictericia neonatal Neonatal jaundice caused by galactosemia. Hyperbilirubinemia in the term newborn. Rathi N, Rathi A. Galactosemia presenting as recurrent sepsis. Effects of galactosemia in utero. IBN Publindex Publindex is a Colombian bibliographic index for classifying, updating, rating and certifying scientific and technological publications. Directory of Open Access Journals DOAJ increases the visibility and ease of use of open access scientific and scholarly journals, aims to be comprehensive and cover all that journals that use a quality control system to guarantee the content.
Scopus Scopus is a bibliographic directta publishing summaries and hiperbilirrubbinemia concerning articles from scientific journals. Latindex Latindex is the product of cooperation by a network of Latin-American institutions operating in a coordinated way to gather and disseminate bibliographic information about serialised scientific publications produced in the region.