Neonatal Hyperbilirubinemia
Mostrando 1-12 de 20 artigos, teses e dissertações.
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1. Drug utilization study in neonatal intensive care unit at tertiary care hospital
SUMMARY OBJECTIVE: Neonates are more susceptible to drug interactions and adverse effects, and special care should be taken when prescribing medication to them. This study aimed to investigate drug usage in the neonatal intensive care unit of a tertiary care hospital. METHODS: This prospective observational study was conducted on 98 patients at the Apollo
Revista da Associação Médica Brasileira. Publicado em: 2022
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2. Cord blood bilirubin and prediction of neonatal hyperbilirubinemia and perinatal infection in newborns at risk of hemolysis
Abstract Objective To assess the accuracy of umbilical cord bilirubin values to predict jaundice in the first 48 h of life and neonatal infection. Method Newborn infants treated at a regional well-baby nursery born at ≥36 weeks of gestation were included in this retrospective cohort study. All infants born in a 3-year period from mothers with O blood typ
J. Pediatr. (Rio J.). Publicado em: 2021-08
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3. Reply to Letter to the Editor - Association between sleep behavior and motor development in preterm infants
Abstract Objective To assess the accuracy of umbilical cord bilirubin values to predict jaundice in the first 48 h of life and neonatal infection. Method Newborn infants treated at a regional well-baby nursery born at ≥36 weeks of gestation were included in this retrospective cohort study. All infants born in a 3-year period from mothers with O blood typ
J. Pediatr. (Rio J.). Publicado em: 2021-08
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4. A case of severe glutathione synthetase deficiency with novel GSS mutations
Glutathione synthetase deficiency (GSSD) is a rare inborn error of glutathione metabolism with autosomal recessive inheritance. The severe form of the disease is characterized by acute metabolic acidosis, usually present in the neonatal period with hemolytic anemia and progressive encephalopathy. A case of a male newborn infant who had severe metabolic acido
Braz J Med Biol Res. Publicado em: 11/01/2018
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5. Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
Introduction Auditory neuropathy/dyssynchrony (AN/AD) comprises a spectrum of pathology affecting the auditory pathways anywhere from the inner hair cells to the brainstem. It is characterized by an absent or atypical auditory brainstem response (ABR) with preservation of the cochlear microphonics and/or otoacoustic emissions (OAEs).
Int. Arch. Otorhinolaryngol.. Publicado em: 2015-06
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6. Polimorfismos nos genes das proteínas transportadoras de ânions orgânicos na hiperbilirrubinemia neonatal : um estudo de casos e controles
Jaundice usually is a physiological phenomenon among newborns; however, severe hyperbilirubinemia occurs in 5% to 6% of this population. It has been suggested that genetic variation in the genes of bilirubin transporters could enhance the risk of hyperbilirubinemia when co-expressed with other icterogenic conditions. The present study included newborns with
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 2012
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7. A novel c.197T ® A variant among Brazilian neonates with glucose-6-phosphate dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase (G6PD, EC 1.1.1.49) deficiency is the most common enzyme deficiency worldwide, causing a spectrum of diseases including neonatal hyperbilirubinemia and acute or chronic hemolysis. We used the methemoglobin reduction test and G6PD electrophoresis to screen 655 neonates (354 females and 301 males) for common G6PD mutations in
Genetics and Molecular Biology. Publicado em: 2008
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8. Deficiência auditiva e seus fatores de risco em neonatos e lactentes: estudo em hospital público de Belo Horizonte
The neonatal hearing screening is an important tool for early detection of hearing impairment in children; the objective is the early intervention to avoid language and learning disorders. Hearing impairment has a high prevalence in neonates and should be treated as a Public Health problem. The characterization of risk factors associated with hearing loss is
Publicado em: 2006
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9. Analise da triagem auditiva por audiometria automatica de tronco encefalico de recem-nascidos internados em unidade de cuidados intensivos e intermediarios
The purpose of the present study was to check the prevalence of hearing impairment in newborns hospitalized at the Neonatal MCU, Medical School, University of Campinas, and analyze the risk indicators. We assessed 979 newborn babies using Automatic Auditory Brainstem Response (AABR) between January 2000 and January 2003, using the device branded ALGO, model
Publicado em: 2004
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10. Transient Familial Neonatal Hyperbilirubinemia*
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11. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
Severe jaundice leading to kernicterus or death in the newborn is the most devastating consequence of glucose-6-phosphate dehydrogenase (EC 1.1.1.49; G-6-PD) deficiency. We asked whether the TA repeat promoter polymorphism in the gene for uridinediphosphoglucuronate glucuronosyltransferase 1 (EC 2.4.1.17; UDPGT1), associated with benign jaundice in adults (G
The National Academy of Sciences of the USA.
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12. Prolonged Neonatal Unconjugated Hyperbilirubinemia Associated with Breast Feeding and a Steroid, Pregnane-3 (Alpha), 20 (Beta)-Diol, in Maternal Milk That Inhibits Glucuronide Formation In Vitro*