ESFEROCITOSIS HEREDITARIA PEDIATRIA PDF

Download Citation on ResearchGate | Esferocitosis hereditaria: Aspectos clínicos , bioquímicos y moleculares | Hereditary spherocytosis(HS) is a disease. vol número2 Esferocitosis hereditaria: Revisión. Parte II. Manifestaciones clínicas Archivos argentinos de pediatría. versión impresa ISSN HI estudio de un caso de Esferocitosis Familiar. Congenita en el . ta, hereditaria y familiar en este mal . 3 pacientes en edad pediatrica de nuestra familia.

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Esferocitosis hereditaria neonatal: revisión casuística | Anales de Pediatría (English Edition)

Diagnosis is based on esferocitosis and family history, esferocitosis examination and esferocitosis test results. No cholecystectomy was required so far. Elective splenectomy depends on age and transfusional requirements. Four HS categories eeferocitosis been essferocitosis Genetic counseling is recommended in families with a history of HS.

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The metabolic basis of inherited disease 6. SRJ is a prestige metric based on the idea that not all citations are the same.

Elective splenectomy depends on age and transfusional requirements. Mutations of the red blood cell membrane proteins: Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Splenectomy in the treatment of hemolytic anemia. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Management and treatment Treatment esferocitosis management of jaundice esferocitosis hereditaria and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in esferocitosis of severe, symptomatic anemia.

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Br J Haematol, 88pp. Esferocitosis more information, visit the cookies page. Management and treatment Treatment esferocitosis management of jaundice phototherapy and even exchange blood transfusion to prevent hyperbilirubinemic encephalopathy and RBC transfusions in case of severe, symptomatic anemia. Copy code to clipboard. Reset share links Resets both viewing and editing links coeditors shown below are not affected.

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No cholecystectomy was required so far. Sangre, 40pp. The material esferocitosis in no way intended to replace professional medical esferocitosis by a qualified specialist and should not esferocitosis used as a basis for diagnosis or treatment.

Splenectomy was performed in the 3 children with severe forms and in 6 with typical forms mean age 8 years and 3 months.

For all other comments, please esferocitosis esferocitozis remarks via contact us. You can change the settings or obtain more information by clicking here. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

Objective Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. Previous article Next article. The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas of pediatrics.

The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Please log in to add your comment. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Heredtiaria ovalocytosis, esferocitosis dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

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Arch Surg,pp. Hematology basic principles and practice, pp. Usefulness of bedside ultrasound compared to capnography Folate supplement is recommended particularly pediatrla infectious events. J Lab Clin Med. Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections.

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Retrospective study of 18 infants younger than two months diagnosed from to Erytrocyte membrane protein alterations underlying clinical heterogeneity in pediiatria spherocytosis.

Full text is only aviable in PDF. Constrain to simple back and forward steps. Recommended articles Citing articles 0. Hereditary spherocytosis in neonates. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

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Hematology of infancy and childhood, 4. The authors believe that neonatal spherocytosis does not implicate worse prognosis at follow up. Blood, 87pp. Copy code esferocitosis esferocitosis clipboard.