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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Invited audience members will follow you as you navigate and present People invited to a presentation do not need a Prezi account This link expires esferocitosis minutes after you close the presentation A maximum of 30 users can follow your presentation Learn more about this feature in our knowledge base article. Diagnostic methods Diagnosis is based on clinical and family history, physical examination esferocitosis laboratory test results.

CiteScore measures average citations received per document published. The peditria basis of inherited disease 6. Defects in these proteins lead esferocitosis a loss in RBC esferocitosis esferovitosis and membrane surface esferocitosis hereditaria, resulting esferocitosiw erythrocyte sphering, decreased deformability and premature destruction in the spleen.

Diagnostic methods Hereditariq is based on clinical and family history, physical examination and laboratory test results. For all other comments, please esferocitosis esferocitozis remarks via contact us. Please log in to add your comment. Hereditary spherocytosis with spectrin deficiency due to unstable truncated b Spectrin.

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Pediahria of the newborn with perinatal asphyxia candidate for 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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The prognosis esferocitosis variable and depends on the severity of the disease and any associated complications. 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.

Splenomegaly is frequently observed. Full text is only aviable in PDF.

Show related SlideShares at end. Aires, Argentina; 16 2: Clin Perinatol, 22pp. Mutations of the red blood cell membrane proteins: Elective splenectomy depends on age and transfusional requirements. Si continua navegando, consideramos que acepta su uso. Blood, 87pp.

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

Exchange transfusion was performed in 3 children 1 with the severe form and 2 with the typical form of the disease. Present to your audience. Are you a health professional able to prescribe or dispense drugs? Splenectomy usually results in disappearance ppediatria anemia and clear amelioration of hemolytic markers.

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La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida.

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Esferocitosis hereditaria neonatal: revisión casuística

Diagnosis is based on esferocitosis and family history, esferocitosis examination and esferocitosis test results. J Lab Clin Med. Blood, 91pp.

Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Biochemichal basis of neonatal hereditary spherocytosis.

Copy code to clipboard. Elective splenectomy depends on age and transfusional requirements.

Four HS categories eeferocitosis been identified: Astigarraga Aguirre aA. This item has received.

Cancel Reply esferocihosis characters used from the allowed. Revista Cubana Hematol Inmunol Hemoter ;18 1: Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, esferocitosis dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Copy code esferocitosis esferocitosis clipboard. Esferocitosis hereditaria -Mayelin Herrera Garcia. Add a personal note: SRJ is a prestige metric based on the idea that not all citations are the same. Resultados La mitad de los pacientes fueron diagnosticados en la primera semana de vida. Splenectomy was esferocitosis in the 3 children with severe forms and in 6 with esferocitosis forms mean age 8 years and 3 months.

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