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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Revista Cubana Hematol Inmunol Hemoter ;18 1: The Italian survey on hereditary spherocytosis.

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Int J Pediatr Hematol Oncol ; 2: Blood Cells Mol Dis ; Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases.

Oxygen affinity and compensated hemolysis in hereditary spherocytosis. J Lab Clin Med. Eesferocitosis, Argentina; 16 2: Clinico-hematological profile of hereditary spherocytosis: Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: Am J Hematol ;57 1: Postoperative pulmonary embolism in a young female accompanying with Factor V Leiden mutation and hereditary sypherocytosis.


Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

J Thromb Thrombolysis ;17 3: Journal of Medical Cases. Hereditary Spherocytosis in Neonates with Hyperbilirubinemia.

Guidelines for the diagnosis and management of hereditary spherocytosis update. 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.

Thrombo-embolic disease after splenectomy for hereditary stomatocytosis. Br J ;or ;93 2: Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.

Splenectomy for hereditary spherocytosis: Laparoscopic partial vs total splenectomy in children with hereditary spherocytosis. Servicio de ayuda de la revista.

Referencias -Mayelin Herrera Garcia.