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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Investigation of neurodevelopment delay etiology: 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. With a transversal and prospective method, six groups were identified: 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.

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It is emphasized the specialist evaluation, and the need of appropriate flow of information in the net of health. Ultrassonografia transfontanelar neonatal foi realizada em 4 das 22, sendo normal em uma. Neonatal encephalopathy following fetal distress: Leviton A, Nelson KB. Problems with definitions and classifications of newborn encephalopathy.

Rev Bras Ginecol Obst ; Factors identified during the neonatal period associated kernixterus risk of cerebral palsy.

Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: Neurology of the newborn, 3 rd edition. Periventricular leukomalacia of infancy: Limitations of ultrasonography for diagnosing white matter cusas in preterm infants.

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BJOG ; Suppl Prenatal cytomegalovirus disease and cerebral microgyria: Clinical-neurologic, cytogenetic and molecular aspects of the Prader-Willi and Angelman syndromes.

A further case of a Prader-Willi syndrome phenotype in a kednicterus with Angelman syndrome molecular defect. Strategies for preimplantation genetic diagnosis of Angelman syndrome caused by mutations in the UBE3A gene. Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.

Benign idiopathic external hydrocephalus benign subdural collection in 39 children: Etiologic determination of childhood developmental delay.

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Clinical analysis of children with developmental delay.

Investigation of neurodevelopment delay etiology: resources and challenges

Chang Gung Med J ; Medical management of neurofibromatosis 1: J Am Acad Dermatol ; Assessing alcohol misuse during pregnancy: J Stud Alcohol ; Diagnosis of fetal infections.

Curr Opin Obstet Gynecol ; Social support and infant malnutrition: Recebido 26 Agostorecebido na forma final 16 Janeiro Aceito 22 Fevereiro All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Services on Demand Journal. 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.

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