Esferocitosis hereditaria. Carolina Cózar Trastorno hemolítico familiar caracterizado por: anemia ictericia intermitente esplenomegalia. Esferocitosis Hereditaria Anemia Esferocitosis Hereditaria 1) Defecto de la membrana del eritrocito. 2) Retención selectiva por el bazo normal. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la Las manifestaciones clínicas como ictericia, esplenomegalia, anemia, aplasia y y sobrecarga de hierro sugiere daño pancréatico por la acumulación, tal como se.
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Clinico-hematological profile of hereditary spherocytosis: J Thromb Thrombolysis ;17 3: Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.
Am J Hematol ;57 1: Polish Academjy of Sciences? J Lab Clin Med. King on behalf of the General Haematology Task Force of the British Committee for Standards in Haematology Esferociosis for the diagnosis and management of hereditary spherocytosis. Este hecho explica la discrepancia entre estos valores. Blood Cells Mol Dis ; A study of 62 Spanish cases. Aires, Argentina; 16 2: Se recomienda el wnemia de glucemia y ferritina.
Anemia Esferocitosis Hereditaria by Danna flores cuadros on Prezi
The identity of hyperchromic RBC and spherocytes as well as their normal esferlcitosis have been previously established. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Thrombo-embolic disease after splenectomy for hereditary stomatocytosis.
This explains the discrepancy between these values. Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis.
Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis. Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. Monitoring of blood glucose and ferritin is recommended.
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Revista Cubana Hematol Inmunol Hemoter ;18 1: Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. Thus opr becomes possible to screen for both hereditary and secondary spherocytosis. Hereditary Spherocytosis in Neonates with Hyperbilirubinemia.
Referencias -Mayelin Herrera Garcia. Int J Pediatr Hematol Oncol ; 2: Journal of Medical Cases.
Guidelines for the diagnosis and management of hereditary spherocytosis update. Applying criteria such as permanence of an increased percentage of spherocytes, family history, biochemical symptoms of hemolysis and clinical data, we claim a prevalence of generally asymptomatic hereditary spherocytosis HS of 1: The Italian survey on hereditary spherocytosis.
Erythroid membrane protein defects in hereditary spherocytosis. The high association of HS with both diabetes and iron overload suggest damage of the endocrine pancreas by the latter, as it is also seen in genetic hemochromatosis. Oxygen affinity and compensated hemolysis in hereditary spherocytosis.
Br J Haematol ;93 2: HS being a hemolytic defect, frequently increased iron overload was not unexpected. Abstract Hematological automates using double beam laser diffraction by artificially spherized red blood cells determine both volume and hemoglobin concentration of a very large number of cells, even indicating percentages of aberrant elements.
Servicio de ayuda de la revista. Splenectomy for hereditary spherocytosis: