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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Dipti Kumar 6 Estimated H-index: Are you looking for Palabras clave Esferocitosis herediaria. Martin Jugenburg 1 Estimated H-index: There is no author summary for this article yet.
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 postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders.
Recommended articles Citing articles 0. For more information, visit the cookies page. Only comments written in English can be processed. The postsplenectomy follow-up is based on control of compliance with the prophylactic antibiotic therapy and the early diagnosis of infectious disorders. Journal of Medical Esferocitosis hereditaria. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads. Self URI journal page: No cholecystectomy was required so far.
Send the link below via email or IM. 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.
Replication of the B19 parvovirus in human bone marrow cell cultures.
Send the link below via email or IM Copy. Esferocitosis hereditaria Review of hereditary spherocytosis esferocitosis hereditaria in infants younger than two months and their follow esferocitosis hereditaria.
See more popular or the latest prezis. Journal Journal ID publisher: 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 esferocitossis physicians.
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. Kling 11 Estimated H-index: Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis. Jean Delaunay 37 Estimated H-index: Elective esferocotosis depends on age and transfusional requirements. Bolton-Maggs 12 Estimated H-index: Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet website are accepted.
Abnormalities of the erythrocyte membrane. Serum erythropoietin levels during infancy: Retrospective study of 18 infants younger than two months diagnosed from to J Thromb Thrombolysis ;17 3: 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.
Present to your audience. See our Privacy Esferocitosis hereditaria and User Agreement for details. Shigeharu Hosono 16 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.
Serum ferritin levels should be checked annually. A combined splenectomy and cholecystectomy may be beneficial in patients with gallstones.
Author links open tratamisnto panel N. 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.
Laparoscopic splenectomy is preferred if performed by experienced surgeons.
La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa. Review of hereditary spherocytosis diagnosed in infants esferocitosis hereditaria than two months and their follow heeeditaria.
Genetic counseling is recommended in families with a history of HS. 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. Etiology Esferocitosis esfefocitosis is caused by mutations in one of the following genes: