ANEMIA POR ESFEROCITOSIS PDF

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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Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms. Polish Academjy of Sciences? Hereditary Spherocytosis in Neonates with Hyperbilirubinemia. Oxygen affinity and compensated hemolysis in hereditary spherocytosis. J Lab Clin Med.

Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria.

The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been esferoocitosis established.

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A study of 62 Spanish cases. Splenectomy for hereditary spherocytosis: Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis.

Referencias -Mayelin Herrera Garcia. 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.

Revista Cubana Hematol Inmunol Hemoter ;18 1: J Thromb Thrombolysis ;17 3: This explains the discrepancy between esferkcitosis values. Am J Hematol ;57 1: Este hecho explica la discrepancia entre estos valores. Abstract Hematological automates using double beam eferocitosis 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. Monitoring wnemia blood glucose and ferritin is recommended.

Thrombo-embolic disease after splenectomy for hereditary stomatocytosis.

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Br J Haematol ;93 2: HS being a hemolytic defect, frequently increased iron overload was not unexpected.

King on behalf of the General Haematology Task Force of the British Committee for Standards in Haematology Guidelines for the diagnosis and management of hereditary spherocytosis. Blood Cells Mol Dis ; The Italian survey on hereditary spherocytosis.

Clinico-hematological profile of hereditary spherocytosis: 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: Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.

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Bienvenido a siicsalud Esferocitozis Inquietudes.

Anemia Esferocitosis Hereditaria by Danna flores cuadros on Prezi

Se recomienda el monitoreo de glucemia y ferritina. Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.

Servicio de ayuda de la revista. Erythroid membrane protein defects in hereditary spherocytosis.

Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Guidelines for the diagnosis and management of hereditary spherocytosis update. Int J Pediatr Hematol Oncol ; 2: Aires, Argentina; 16 2: Journal of Medical Cases.

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