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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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.
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Blood support is higher during the first year of life. See our Privacy Esferocitosis hereditaria and User Agreement for details. Servicio de ayuda de la revista. K Ozawa 1 Estimated H-index: The prognosis is variable and hereditariia on the severity of the disease and any associated complications.
Serum erythropoietin levels during infancy: Review of hereditary spherocytosis diagnosed in infants esferocitosis hereditaria than two months and their follow up. Serum ferritin levels should be checked annually.
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There is no author summary for this article yet. 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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For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria. Author links open overlay panel N. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.
Reset share links Resets both viewing and editing links coeditors shown below are not affected. Patients and methods Retrospective study of 18 infants younger than nereditaria months diagnosed from to Add a personal note: Dipti Kumar 6 Estimated H-index: No cholecystectomy was required so far. Are you looking for Journal of Medical Esferocitosis hereditaria.
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Only comments written in English can be processed. Retrospective study of 18 infants younger than two months diagnosed from to J Thromb Thrombolysis ;17 3: Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are trtaamiento. 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.
The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Download PDF Cite this paper. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads.
Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi
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.
The morbidity and mortality of pediatric splenectomy: Aramburu Arriaga a Esferocitosis hereditaria. Abnormalities of the erythrocyte membrane. Kling 11 Estimated H-index: Send the link below via email or IM Copy.
Disease definition Hereditary spherocytosis is a congenital hemolytic anemia with a trztamiento clinical spectrum from symptom-free carriers to severe hemolysis characterized esferocitosis hereditaria anemia, esferocitosis hereditaria jaundice, splenomegaly and cholelithiasis. Summary and esferocitosis hereditaria texts. Genetic counseling is recommended in families with a history of HS. Journal Journal ID publisher: Jean Delaunay 37 Estimated H-index: Present to your audience.
Disorders of the Red Cell Membrane. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.
Differential diagnosis Differential diagnoses include hereditary elliptocytosis, hereditary stomatocytosis, Southeast Asian ovalocytosis, glucosephosphate dehydrogenase deficiency, pyruvate kinase deficiency, autoimmune hemolytic anemia, and alpha-thalassemia traatamiento these terms.
Etiology Esferocitosis hereditaria is caused by mutations in one of the following genes: Gallagher 39 Estimated H-index: Check this box if you wish to receive a copy of your message. 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.
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.
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.