CAUSAS DE KERNICTERUS PDF

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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With a transversal and prospective method, six groups were identified: Assessing alcohol misuse during pregnancy: The McGraw-Hill Companies; Kernicterus is the syndrome that occurs if acute bilirubin encephalopathy causes permanent damage to the brain. How to cite this article. An underlying disorder may cause infant jaundice. 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, kermicterus 1 to 47 months age, between andattending a Stimulation Program of the Association of Parents and Friends of Exceptional Children of Batatais-SP.

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Ictericia infantil – Síntomas y causas – Mayo Clinic

Prenatal cytomegalovirus disease krrnicterus cerebral microgyria: Prompt treatment may prevent significant lasting damage. Escrito por el personal de Mayo Clinic. Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene. Los principales factores de riesgo de ictericia, particularmente la ictericia grave, que pueden causar complicaciones comprenden los siguientes:.

Clinical analysis of children with developmental delay. La ictericia nuclear puede provocar lo siguiente:.

Investigation of neurodevelopment delay etiology: resources and challenges

A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect. Clinical-neurologic, cytogenetic and molecular aspects of the Prader-Willi and Angelman syndromes.

Kkernicterus on Demand Journal. J Stud Alcohol ; 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.

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Diagnosis of fetal infections. Periventricular leukomalacia of infancy: Hay WW, et al. Call your doctor if:.

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American Academy of Pediatrics Policy. Neurology of the newborn, 3 rd edition. Bilirubin is toxic to cells of the brain.

Ultrassonografia transfontanelar neonatal foi realizada em 4 das 22, sendo normal em uma. 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.

Medical management of neurofibromatosis 1: Rev Bras Ginecol Obst ; Leviton A, Nelson KB.

Chang Gung Med J ; Curr Opin Obstet Gynecol ; Etiologic determination of childhood developmental delay. Investigation of neurodevelopment delay etiology: