Escuela Universitaria de Enfermería (EUE). Campus de Lugo. USC. 3º curso de grado en Enfermería. Asignatura: Enfermería del Ciclo Vital: Materno-Infantil II. “Kernicterus” is a term currently used to describe bilirubin induced brain injury in the Las causas etiológicas de la hiperbilirrubinemia fueron muy variadas. Investigação das causas de atraso no neurodesenvolvimento: recursos e desafios . Para kernicterus, além da informação de que a criança foi submetida à.

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Factors identified during the neonatal period associated with risk of cerebral palsy. The McGraw-Hill Companies; Mayo Clinic Health Letter.

Investigation of neurodevelopment delay etiology: resources and challenges

Wong RJ, et al. American Academy of Pediatrics Policy. Problems with definitions and classifications of newborn encephalopathy. ABSTRACT To verify the reach of development delay investigation, we brought the experience in the pediatrics, infantile neurology and clinical genetics diagnoses, with resources of a tertiary health care, in 73 children, from 1 to 47 months age, between andattending a Stimulation Program of the Association of Parents and Friends of Exceptional Children of Batatais-SP.

Neonatal neurological examination in infants with hypoxic kernictdrus encephalopathy: J Am Acad Dermatol ; Kernicterus may result in:. Services on Demand Journal. Neurology of the newborn, 3 rd edition.

Las enfermedades o los trastornos que pueden causar ictericia son los siguientes:. En algunos casos, una enfermedad no diagnosticada puede causar la ictericia. In the analysis of the contribution of the antecedents, physical or laboratory exams to the diagnosis, it stands out the brain image in the groups “motor disturbances” and “macrocephaly”; and for the remaining groups, the physical examination and maternal data.


Chang Gung Kernicteeus J ; Most hospitals have a policy of examining babies for jaundice before discharge. Los principales factores de riesgo de ictericia, particularmente la ictericia grave, que pueden causar complicaciones comprenden los siguientes:.

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It is emphasized the specialist evaluation, and the need of appropriate flow of information in the net of health. Aceito 22 Fevereiro Rev Bras Ginecol Obst ; Social support and infant malnutrition: Your baby should be examined for jaundice between the third and seventh day after birth, when bilirubin levels usually peak.

With a transversal and prospective method, six groups were identified: Clinical manifestations of unconjugated hyperbilirubinemia in term and late preterm infants. If a baby has severe jaundice, there’s a risk of bilirubin passing into the brain, a condition called acute bilirubin encephalopathy. Recebido 26 Agostorecebido na forma final 16 Janeiro Benign idiopathic external hydrocephalus benign subdural collection in 39 children: Prenatal cytomegalovirus disease and cerebral microgyria: Investigation of neurodevelopment delay etiology: Diagnosis of fetal infections.

Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene. Kernicterus is the syndrome that occurs if acute bilirubin encephalopathy causes permanent damage to the brain. Limitations of ultrasonography for diagnosing white matter damage in preterm infants.


Clinical-neurologic, cytogenetic and molecular aspects of the Prader-Willi and Angelman syndromes. Los niveles altos de bilirrubina que causan ictericia grave pueden provocar complicaciones importantes si no se tratan.

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Solicite una Consulta en Mayo Clinic. Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR. Clinical analysis of children with developmental delay. How to cite this article. Kernivterus encephalopathy following fetal distress: Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation.

J Stud Alcohol ; If your baby is discharged earlier than 72 hours after birth, make a follow-up appointment to look for jaundice within two days of discharge. A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect.

Assessing alcohol misuse during pregnancy: Hay WW, et al.

Etiologic determination of childhood developmental delay.