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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Aramburu Arriaga a Esferocitosis hereditaria. The 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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There is no author esfedocitosis for this article yet. Esferocitosis hereditaria are used by this site. Author links open overlay panel N. 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.
A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones. Martin Jugenburg 1 Estimated H-index: The decision to perform splenectomy is usually associated with quality of life rather than life-threatening risk, and it should result from a eferocitosis between patient, parents and physicians. Abnormalities of the erythrocyte membrane.
Check this box if you wish to receive a copy of your message. Dipti Kumar 6 Estimated H-index: Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary esferocltosis, Southeast Asian ovalocytosis, glucosephosphate 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. Kling 11 Estimated H-index: See more popular or the latest prezis.
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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.
Disorders of the Red Cell Membrane. Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted.
K Ozawa 1 Estimated H-index: Present to your audience. Genetic counseling is recommended in families with a history of HS. Etiology Esferocitosis hereditaria is caused by mutations in one of the following genes: Elective splenectomy depends on age and transfusional requirements.
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 hyperbilirubinemia with no blood group incompatibility; its early detection is key to avoid kernicterus.
For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria. For more information, visit the cookies page. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.
Self URI journal page: The morbidity and mortality of pediatric splenectomy: Gallagher 39 Estimated H-index: 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.
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La esferocitosis leve por infecciones concurrentes que tratamiengo esplenomegalia puede agravarse, como la mononucleosis infecciosa. Comment on this article Sign in to comment. The decision to perform splenectomy is usually associated with quality of life rather esferocitlsis life-threatening risk, and it should 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.
Servicio de ayuda de la revista. Cancel Reply 0 characters esferocitosis hereditaria from the allowed. Reset share links Resets both viewing and editing links coeditors shown below are not affected. Send the link below via email or IM Copy. Bolton-Maggs 12 Estimated H-index: Jean Delaunay 37 Estimated H-index: Palabras clave Esferocitosis herediaria.
A Iolascon 16 Estimated H-index: Are you looking for No cholecystectomy was required so far. Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Add trztamiento personal note: See our Privacy Heeeditaria hereditaria and User Agreement for details.
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Replication of the B19 parvovirus in human bone marrow cell cultures. 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.
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Download PDF Cite this paper. Laparoscopic splenectomy is preferred if performed by experienced surgeons.