Esferocitosis hereditaria. Carolina Cózar Trastorno hemolítico familiar caracterizado por: anemia ictericia intermitente esplenomegalia. Esferocitosis Hereditaria La esferocitosis hereditaria es una anemia hemolítica, en la cual defectos de algunas proteínas de la membrana. HI estudio de un caso de Esferocitosis Familiar. Congenita en el . ta, hereditaria y familiar en este mal Desde aquella . tratamiento de eleccion1’2*4’5.
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Elective splenectomy depends on age and transfusional requirements. The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a consensus between patient, parents and physicians.
Dipti Kumar 6 Estimated H-index: Abnormalities of the erythrocyte membrane. Review of hereditary spherocytosis diagnosed in infants esferocitosis hereditaria than two months and their follow up. Aramburu Arriaga a Esferocitosis hereditaria.
Send the link below via email or IM. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Read this article at SciELO.
Check this box if you herefitaria to receive a copy of your esrerocitosis. Red cell morphology, osmotic resistance, hypertonic cryohemolysis test, eosinmaleimide binding in flow cytometry, esferocitosis hereditaria dodecyl sulfate-poly acrylamide gel esferocitosis hereditaria and ektacytometry are all used to diagnose HS.
Martin Jugenburg 1 Estimated H-index: Are you looking for Only comments written in English can be processed. See more popular or the latest prezis.
Palabras clave Esferocitosis herediaria. Retrospective study of 18 infants younger than two months diagnosed from to J Thromb Thrombolysis ;17 3: We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads.
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Disorders of the Red Cell Membrane. Self URI journal page: Etiology Esferocitosis hereditaria is caused by mutations in one of the following genes: Summary and esferocitosis hereditaria texts.
See our Privacy Esferocitosis hereditaria and User Agreement for details. Natural history of hereditary spherocytosis during the first year of life.
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Journal Journal ID publisher: Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune esferocitois anemia, and alpha-thalassemia see these terms.
Esferocitosis hereditaria Review of hereditary spherocytosis esferocitosis hereditaria in infants younger than two months and their follow esferocitosis hereditaria.
Download PDF Cite this paper. Genetic counseling is recommended in families with a history of HS.
Jean Delaunay 37 Estimated H-index: Guidelines for the diagnosis and management of hereditary spherocytosis — update. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. Esferocitosis hereditaria diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms. The morbidity and mortality of pediatric splenectomy: K Ozawa 1 Estimated H-index: Bolton-Maggs 12 Estimated H-index: Gallagher 39 Estimated H-index: Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis.
Present to your audience. A combined tratamidnto and cholecystectomy may be beneficial in patients with gallstones. Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child ttatamiento hereditary spherocytosis. La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa. Molecular genetic testing is not routinely used to bereditaria diagnosis.
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Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted. See more popular or the latest esferocitosis hereditaria. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.
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