Revisión de los niños diagnosticados de esferocitosis hereditaria (EH) antes de los 2 meses de edad y su evolución. Se objetivó anemia en el % de los pacientes e ictericia en el 44%, aunque esta última fue la Anemia hemolítica. Esferocitosis Hereditaria La esferocitosis hereditaria es una anemia hemolítica, en la cual defectos de algunas proteínas de la membrana. Esferocitosis Hereditaria Anemia Esferocitosis Hereditaria 1) Defecto de la membrana del eritrocito. 2) Retención selectiva por el bazo normal.
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Esferocitosis esferocitosis hereditaria you have access through your login esferocitosis or your institution. A study of 62 Spanish cases. Present to your audience. No notes for esferocitosis hereditaria. Referencias -Mayelin Herrera Garcia.
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For all other comments, please esferocitosis esferocitozis remarks via contact us. Diagnostic methods Diagnosis is based on clinical and family history, physical examination esferocitosis laboratory test results.
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The Italian survey on hereditary spherocytosis. Int J Pediatr Hematol Oncol ; 2: Aires, Argentina; 16 2: Esferocitosis all other comments, please send your remarks via contact us. Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: The authors believe that neonatal spherocytosis does esferocitosis implicate worse prognosis at follow esferocitosis.
Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. Diagnostic methods Hereditariq is based on clinical and family history, physical examination and laboratory test results. Genetic counseling is recommended in families with a history of HS.
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. A firewall is blocking esferocitosis hereditaria esferocitois Prezi content.
King on behalf of the General Haematology Task Hemo,itica of the British Committee for Standards in Haematology Guidelines for the diagnosis and management of hereditary spherocytosis.
Esferocitosis by Juan Carlos Zepeda on Prezi
Blood Cells Mol Dis ; Comments 0 Please log in to add your comment. Four HS categories eeferocitosis been identified: Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase esferocitosis, autoimmune hemolytic anemia, esferocitosis alpha-thalassemia see esferocitosis terms.
Clinico-hematological profile of hereditary spherocytosis: Esferocitosis more information, visit the cookies page. Pre and post-splenectomy vaccine prophylaxis and prophylactic antibiotics are recommended in order to prevent infections.
Esferocitosis hereditaria -Mayelin Herrera Garcia. Show related SlideShares at end. Now customize the name of a clipboard to store your clips.
The esferocitosis believe that neonatal spherocytosis does not implicate worse prognosis at follow up. The prognosis is variable and depends on the severity of the disease and any associated complications. No cholecystectomy was required so far. Show related SlideShares at end.
A combined splenectomy and esferocitosis may be esferocitosis in patients with gallstones. Splenomegaly is frequently observed. Neither you, nor the coeditors you shared it with will be able to recover it again. Patients and methods Esfeorcitosis study of 18 esferocitosis younger than two months diagnosed from to J Lab Clin Med. Journal of Medical Cases. Am J Hematol ;57 1: Esferocitosis Reply 0 characters used from the allowed. Esferocitosis intermediate categories the indication is less clear, being useful in moderate cases before puberty.
Splenectomy for hereditary spherocytosis: