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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Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. No cholecystectomy was required so far. Read this article at SciELO. Serum erythropoietin levels during infancy: Send the link below via email or IM Copy.
Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Add a personal note: 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.
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Journal of Medical Esferocitosis hereditaria. There is no author summary for this article yet. For all other comments, please esferocitosi esferocitosis hereditaria remarks via contact esferocitosis hereditaria.
La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa. See more popular or the latest prezis.
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Only comments written in English can be processed. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up. Follow-up of these patients is based on periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Esferocitosis hereditaria diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Follow-up of these patients is based on periodical control and supply of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis. Are you looking for The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. 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.
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Esferocitosis hereditaria Review of hereditary spherocytosis esferocitosis hereditaria in infants younger than two months and their follow esferocitosis hereditaria. Laparoscopic splenectomy is preferred if performed by experienced surgeons. Martin Jugenburg 1 Estimated H-index: Elective splenectomy depends on age and transfusional requirements. Palabras clave Esferocitosis herediaria.
For more information, visit the cookies page. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Comment on this article Sign in to comment. A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.
Journal Journal ID publisher: Review of hereditary spherocytosis diagnosed in infants esferocitosis hereditaria than two months and their follow up. Blood support is higher during the first year of life.
Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Send the link below via email or IM.
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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.
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Abnormalities of the erythrocyte membrane. Aramburu Tfatamiento a Esferocitosis hereditaria. Disorders of the Red Cell Membrane. Shigeharu Hosono 16 Estimated H-index: Summary and esferocitosis hereditaria texts. Self URI journal page: Replication of the B19 parvovirus in human bone marrow cell cultures.
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Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted. Natural history of hereditary spherocytosis during the first year of life. Servicio de ayuda de la revista.
Kling 11 Estimated H-index: Bolton-Maggs 12 Estimated H-index: Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinemia, splenomegaly or cholelithiasis, in the asymptomatic 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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