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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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Polish Academjy of Sciences? Este hecho explica la discrepancia entre estos valores. Br J Haematol ;93 2: The identity of hyperchromic RBC and spherocytes as well as their normal percentage have been previously established.

Thrombo-embolic disease after splenectomy for hereditary stomatocytosis. Int J Pediatr Hematol Oncol ; 2: Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis.

Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: Servicio de ayuda de la revista. Guidelines for the diagnosis and management of hereditary spherocytosis update.

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: 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: Clinico-hematological profile of hereditary spherocytosis: Bienvenido a siicsalud Contacto Inquietudes.


The Italian survey on hereditary spherocytosis. J Lab Clin Med. Am J Hematol ;57 1: This explains the discrepancy between these values. Erythroid membrane protein defects in hereditary spherocytosis.

Hereditary Spherocytosis in Neonates with Hyperbilirubinemia. Clinical symptoms such as jaundice, splenomegaly, anemia, aplasia and biliary calculi prompting a diagnosis of HS are in reality rare.

Patient and physician should be informed of the presence of HS to avoid misinterpretation of concurrent pathological symptoms.

Anemia Esferocitosis Hereditaria by Danna flores cuadros on Prezi

Oxygen affinity and compensated hemolysis in hereditary spherocytosis. Journal of Medical Cases. 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. Blood Cells Mol Dis ; Esferocitodis for hereditary spherocytosis: Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

A study of esferocitsis Spanish cases. Referencias -Mayelin Herrera Garcia. Aires, Argentina; 16 2: J Thromb Thrombolysis ;17 3: HS being a hemolytic defect, frequently increased iron overload was not unexpected. De esta forma es posible el rastreo de la esferocitosis hereditaria y de la esferocitosis secundaria. 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.


Monitoring of blood glucose and ferritin is recommended. Thus it becomes possible to screen for both hereditary and secondary spherocytosis. Se recomienda el monitoreo de glucemia y ferritina.