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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The Italian survey on hereditary spherocytosis. Este hecho explica la discrepancia entre estos valores. Splenectomy for hereditary spherocytosis: Se recomienda poe monitoreo de glucemia y ferritina.
Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi
The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established. Referencias -Mayelin Herrera Garcia. Monitoring of blood glucose and ferritin is recommended. Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.
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.
J Thromb Thrombolysis ;17 3: De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. Journal of Medical Cases. J Esferocitodis Clin Med.
Aires, Argentina; 16 2: 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. Int J Pediatr Efserocitosis Oncol ; 2: Am J Hematol ;57 1: Bienvenido a siicsalud Contacto Inquietudes.
Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis. Thrombo-embolic disease after splenectomy for hereditary stomatocytosis.
Hereditary Spherocytosis in Neonates with Hyperbilirubinemia. Revista Cubana Hematol Inmunol Hemoter ;18 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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Hereditary spherocytosis, thrombocytosis, andmia chronic pulmonary emboli: Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.
Clinico-hematological profile of 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. Erythroid membrane protein defects in hereditary spherocytosis. Oxygen affinity and compensated hemolysis in hereditary spherocytosis.
This explains the discrepancy between these values. Blood Cells Mol Dis ; Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Polish Academjy of Sciences? 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: Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.
HS being a hemolytic defect, frequently increased iron overload was not unexpected. A study of 62 Spanish cases. Br J Haematol ;93 2: Servicio de ayuda de la revista.