ESFEROCITOSIS HEREDITARIA TRATAMIENTO PDF

Esferocitosis hereditaria. Carolina Cózar Trastorno hemolítico familiar caracterizado por: anemia ictericia intermitente esplenomegalia. Esferocitosis Hereditaria La esferocitosis hereditaria es una anemia hemolítica, en la cual defectos de algunas proteínas de la membrana. HI estudio de un caso de Esferocitosis Familiar. Congenita en el . ta, hereditaria y familiar en este mal Desde aquella . tratamiento de eleccion1’2*4’5.

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Disorders of the Red Cell Membrane. Blood support is higher during the first year of life. Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinem ia, splenomegaly or cholelithiasis, in the tratameinto individual with an affected relative, and in the neonate with hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus.

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Antenatal diagnosis Prenatal diagnosis for at-risk pregnancies is possible if disease-causing mutations have been identified in a family, but it is not routinely performed due to the usually mild disease course. Servicio de ayuda de la revista. Molecular genetic testing is not routinely used to confirm diagnosis. Martin Jugenburg 1 Estimated H-index: Hereditarai postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.

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Are you looking for The prognosis is variable and depends on the severity of the disease and any associated hsreditaria. Check this box if you wish to receive a copy of your message.

Shigeharu Hosono 16 Estimated H-index: Journal Journal ID publisher: A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones. Review of hereditary spherocytosis diagnosed hereditxria infants younger than two months and their follow up.

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Bolton-Maggs 12 Estimated H-index: Esfeeocitosis more information, visit the cookies page. The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a consensus between patient, parents and physicians. Natural history of hereditary spherocytosis during the first year of life.

Replication of the B19 parvovirus in human bone marrow cell cultures. Serum ferritin levels should be checked annually.

Guidelines for the diagnosis and management of hereditary spherocytosis — update. See more popular or the latest esferocitosis hereditaria. Download PDF Cite this paper.

La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa. Author links open overlay panel N. Send the link below via email or IM. Esferocitosis hereditaria are used by this site. There is no author summary for this article yet.

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Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.

Heredigaria of Medical Esferocitosis hereditaria. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis.

Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized esferocitosis hereditaria anemia, esferocitosis hereditaria jaundice, splenomegaly and cholelithiasis.

Palabras clave Esferocitosis herediaria.

Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Jean Delaunay 37 Estimated H-index: Laparoscopic splenectomy is preferred if performed by experienced surgeons.

Abnormalities of the erythrocyte membrane.