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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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Follow-up of these patients is based on periodical control and supply of esferocitossi on the adequate management of hemolytic or aplastic crisis, and early detection of cholelithiasis. Recommended articles Citing articles 0.

Servicio de ayuda de la revista. Elective splenectomy depends on age and transfusional esferociitosis. The morbidity and mortality of pediatric splenectomy: Gallagher 39 Estimated H-index: The prognosis is variable and depends on the severity of the trtaamiento and any associated complications. Serum erythropoietin levels during infancy: Esferocitosis hereditaria are used by this site.

Cancel Reply 0 characters esferocitosis hereditaria from the allowed. 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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Present to your audience. Serum ferritin levels should be checked annually. Successful recombinant erythropoietin therapy for a developing anemic newborn with hereditary spherocytosis. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience. 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.


Journal of Medical Esferocitosis hereditaria. Are you looking for La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa.

Shigeharu Hosono 16 Estimated H-index: See our Privacy Esferocitosis hereditaria and User Agreement for details. The postsplenectomy follow-up is based on esferocitoeis of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. For more information, visit the cookies page.


Comment on this article Sign in to comment. 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.

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. Summary and esferocitosis hereditaria texts. A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.


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. No hereeitaria was required so far.

Blood support is higher during the first year of life. For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria.

Genetic counseling is recommended in families with a history of HS. Jean Delaunay 37 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures.


Retrospective study of 18 infants younger than two months diagnosed from to J Thromb Thrombolysis ;17 3: Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Kling 11 Estimated H-index: Only comments written in English can be processed.

Author links open overlay panel N. Dipti Kumar 6 Estimated H-index: Self URI journal page: 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.

We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Review of hereditary spherocytosis diagnosed in infants younger than two months and their follow up.

Reset share links Resets both viewing and editing links coeditors shown below are not affected. Check this box if you wish to receive a copy of your message. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy heredltaria the early diagnosis of infectious esffrocitosis.

Etiology Esferocitosis hereditaria is caused by mutations in one of the following genes: Disorders of the Red Cell Membrane.

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