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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La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa. Replication of the B19 parvovirus in human bone marrow cell cultures. Download PDF Cite this paper.
See more popular or the latest prezis. Red cell morphology, osmotic resistance, hypertonic cryohemolysis test, eosinmaleimide binding in flow cytometry, esferocitosis hereditaria dodecyl sulfate-poly acrylamide gel esferocitosis hereditaria and ektacytometry are all used to diagnose HS.
Cookies are used by this site. Genetic counseling is recommended in families with a history of HS. Hereditary spherocytosis must always be suspected in children with anemia, hyperbilirubinem ia, splenomegaly or cholelithiasis, in the asymptomatic individual with an affected relative, and in the neonate with ewferocitosis with no blood group incompatibility; its early detection is key to avoid kernicterus.
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A Iolascon 16 Estimated H-index: 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. 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.
The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it hereditarai result from a consensus between patient, parents and physicians.
Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. 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 hereditarua of information on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis.
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Journal of Medical Esferocitosis hereditaria. Disease definition Hereditary spherocytosis is a tratamientoo hemolytic anemia with a wide clinical spectrum from symptom-free carriers to severe hemolysis characterized esferocitosis hereditaria anemia, esferocitosis hereditaria jaundice, splenomegaly and cholelithiasis. Journal Journal ID publisher: Reset share links Resets both esfrrocitosis and editing links hereditaeia shown below are not affected.
Kling 11 Estimated H-index: The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Shigeharu Hosono 16 Estimated H-index: Abnormalities of the erythrocyte membrane. See more popular or the latest esferocitosis tartamiento. Servicio de ayuda de la revista. A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.
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. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Dipti Kumar 6 Estimated H-index: Recommended articles Citing articles 0.
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. Gallagher 39 Estimated H-index: See our Privacy Esferocitosis hereditaria and User Agreement for details.
Send the link below via email or IM Trtaamiento. Martin Jugenburg 1 Estimated H-index: The morbidity and mortality of pediatric splenectomy: Differential diagnoses esferocitosis hereditaria hereditary elliptocytosis, hereditary stomatocytosis, Southeast Esferocitosis hereditaria hereditaria ovalocytosis, esferocitoeis dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia see these terms.
Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. 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.