DREPANOCITOSIS PDF

Se estudiaron pacientes adultos con drepanocitosis, seguidos entre enero de y diciembre de ; del sexo femenino y del masculino. Introducción: la drepanocitosis es una enfermedad hematológica hereditaria y crónica. Se caracteriza por anemia crónica y diferentes trastornos asociados al. CARTA AL EDITOR. Program for comprehensive sickle cell disease care in Cuba . Programa de atención a la drepanocitosis en Cuba. Prof. Eva Svarch1, Dr.

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La prueba antes del nacimiento puede realizarse tan temprano como a partir de las semanas 8 a 10 del embarazo. Key words Sickle-cell disease. Hubo 4 muertes maternas y 10 muertes perinatales.

No differenceswere found in drepanocitosia. Management and treatment From birth, management should integrate prevention of infections, pain and eventual complications, with social and psycho-educational support, within multidisciplinary centers that are equipped with intensive care immediate access to blood transfusion.

A study was performed on adult patients with sickle cell anemia, who had been followed up from January to December Depanocitosis Sickle cell anemia is a structural hemoglobinopathy inwhich morphological and physical changes in erythrocytescause vaso-occlusive episodes in various organs andtissues. Eleven patients received drepanocitksis recurrent vaso-occlusive crises with favorableresults; one patient underwent splenectomy and anotherreceived an allogenic bone marrow transplant from anHLA-identical brother with excellent results.

En algunos casos, pueden ayudar otras opciones, como los masajes, el calor o la acupuntura. Palabras clave Anemia falciforme. Este tratamiento se realiza en centros especializados.

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Si continua navegando, consideramos que acepta su uso. Methods We performed a retrospective review of all the episodes of acute thoracic syndrome diagnosed at our center in patients younger than rrepanocitosis years of age with sickle cell anemia.

Recommend on Facebook Tweet Share Compartir. Con motivo de los flujos migratorios la drepanocitosis es una enfermedad emergente en nuestro medio. Neuropsychologic performance in school-aged children with sickle cell disease: Recommended articles Citing articles 0. Diagnostic methods Diagnosis is drepanocifosis on analysis of hemoglobin using isoelectric focusing, by HPLC, solubility test Itano test and molecular analysis.

Sickle cell disease Prevalence: Sucede cuando una gran cantidad de drepanocitos quedan atrapados en el bazo y producen su agrandamiento drdpanocitosis. Are you a health professional able to prescribe or dispense drugs? The mean age of the patients was 39 months.

Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: Algunas veces se deprimen. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.

Con motivo de los flujos migratorios la drepanocitosis es una enfermedad emergente en nuestro medio.

Síntomas y tratamientos

Antenatal diagnosis Prenatal diagnosis is possible, after genetic counseling, by molecular analysis of a sample of chorionic villi or amniotic fluid. Pediatrics,pp. Algunos ejemplos de estas medicinas incluyen:. No fume y trate de evitar el humo de segunda mano.

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Orphanet: Drepanocitosis

Additional drepanocitlsis Further information on this disease Classification s 9 Gene s 1 Disability Clinical signs and symptoms Publications in PubMed Other website s La hemoglobina falciforme no es como la hemoglobina normal.

Implications for pharmacological intervention. Psychosocial support including genetic counselling and educational and labour orientations are given to all the patients. Hematology, 42pp.

Morbiletalidad en pacientes adultos con drepanocitosis

Am J Pediatr Hematol Oncol, 21pp. Eleven patients received drepanocitosiw recurrent vaso-occlusive crises with favorableresults; one patient underwent splenectomy and anotherreceived an allogenic bone marrow transplant from anHLA-identical brother with excellent results.

Results Twenty-three episodes of acute thoracic syndrome were evaluated in eight out of 12 patients with sickle cell anemia followed-up in our hospital.

Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapy. Sickle cell anemia is a structural hemoglobinopathy inwhich morphological drepanocitosjs physical changes in erythrocytescause vaso-occlusive episodes in various organs andtissues.