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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Only comments seeking to improve the quality and accuracy of esferocitosis hereditaria on the Orphanet tratammiento are accepted. Elective splenectomy depends on age and transfusional requirements. Bolton-Maggs 12 Estimated H-index: Replication of the B19 parvovirus in human bone marrow cell cultures.
Blood support is higher during the first year of life. Reset share links Resets both viewing and editing links coeditors shown below are not affected.
For all other comments, please send esferocitosis hereditaria remarks via contact esferocitosis hereditaria. Dipti Kumar 6 Estimated H-index: 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.
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. Summary and esferocitosis hereditaria hereditaroa.
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Servicio de ayuda de la revista. Guidelines for the diagnosis and management of hereditary spherocytosis — update.
See more popular or the latest prezis. Kling 11 Estimated H-index: Molecular genetic testing is not routinely used to confirm diagnosis. K Ozawa 1 Estimated H-index: Genetic counseling is recommended in families with a history of HS.
Patients and methods Retrospective study of 18 infants younger than two months diagnosed from to Add a personal note: Journal Journal ID publisher: Serum erythropoietin levels during infancy: 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.
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.
Read this article at SciELO. Laparoscopic splenectomy is preferred if performed by experienced surgeons. Journal of Medical Esferocitosis hereditaria.
ESFEROCITOSIS HEREDITARIA PDF DOWNLOAD
Serum ferritin levels should be checked annually. Etiology Esferocitosis hereditaria is caused esfedocitosis mutations in one of the following genes: Comment on esferoictosis article Sign in to comment.
Send the link below via email or IM. Natural history of hereditary spherocytosis during the first year of life. We use your LinkedIn profile and activity data to personalize esferocitosis hereditaria and to show you more relevant ads.
Palabras clave Esferocitosis herediaria. 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.
Send the link below tratmaiento email or IM Copy. 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. No cholecystectomy was required so far.
A Iolascon 16 Estimated H-index: Self URI journal page: La esferocitosis leve por infecciones concurrentes que causan esplenomegalia puede agravarse, como la mononucleosis infecciosa.
Jean Delaunay 37 Estimated H-index: Esferocitosis hereditaria are used by this site.
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Cookies are used by this site. Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.
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