Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis

Hereditary spherocytosis is the most frequent hereditary anemia excluding beta thalassemia in Argentina. Historical, demographic, genetic and pathogenic aspects of the disease are reviewed, and confirmatory laboratory tests are described. Special characteristics on the outcome of the disease in our...

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Autores principales: Donato, H., Crisp, R.L., Rapetti, M.C., García, E., Attie, M.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03250075_v113_n1_p69_Donato
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spelling todo:paper_03250075_v113_n1_p69_Donato2023-10-03T15:23:15Z Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis Donato, H. Crisp, R.L. Rapetti, M.C. García, E. Attie, M. Flow cytometry Hemolytic anemia Hereditary spherocytosis Hyperbilirubinemia Osmotic fragility Article blood sampling demography hereditary spherocytosis heredity human laboratory test medical history outcome assessment history Spherocytosis, Hereditary Demography History, 19th Century History, 20th Century Humans Spherocytosis, Hereditary Hereditary spherocytosis is the most frequent hereditary anemia excluding beta thalassemia in Argentina. Historical, demographic, genetic and pathogenic aspects of the disease are reviewed, and confirmatory laboratory tests are described. Special characteristics on the outcome of the disease in our population and prevalent protein deficiencies in our country are described. Emphasis is given on new available laboratory tests, which allow an earlier diagnosis using volume of blood samples significantly smaller than required for conventional tests. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03250075_v113_n1_p69_Donato
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Flow cytometry
Hemolytic anemia
Hereditary spherocytosis
Hyperbilirubinemia
Osmotic fragility
Article
blood sampling
demography
hereditary spherocytosis
heredity
human
laboratory test
medical history
outcome assessment
history
Spherocytosis, Hereditary
Demography
History, 19th Century
History, 20th Century
Humans
Spherocytosis, Hereditary
spellingShingle Flow cytometry
Hemolytic anemia
Hereditary spherocytosis
Hyperbilirubinemia
Osmotic fragility
Article
blood sampling
demography
hereditary spherocytosis
heredity
human
laboratory test
medical history
outcome assessment
history
Spherocytosis, Hereditary
Demography
History, 19th Century
History, 20th Century
Humans
Spherocytosis, Hereditary
Donato, H.
Crisp, R.L.
Rapetti, M.C.
García, E.
Attie, M.
Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
topic_facet Flow cytometry
Hemolytic anemia
Hereditary spherocytosis
Hyperbilirubinemia
Osmotic fragility
Article
blood sampling
demography
hereditary spherocytosis
heredity
human
laboratory test
medical history
outcome assessment
history
Spherocytosis, Hereditary
Demography
History, 19th Century
History, 20th Century
Humans
Spherocytosis, Hereditary
description Hereditary spherocytosis is the most frequent hereditary anemia excluding beta thalassemia in Argentina. Historical, demographic, genetic and pathogenic aspects of the disease are reviewed, and confirmatory laboratory tests are described. Special characteristics on the outcome of the disease in our population and prevalent protein deficiencies in our country are described. Emphasis is given on new available laboratory tests, which allow an earlier diagnosis using volume of blood samples significantly smaller than required for conventional tests.
format JOUR
author Donato, H.
Crisp, R.L.
Rapetti, M.C.
García, E.
Attie, M.
author_facet Donato, H.
Crisp, R.L.
Rapetti, M.C.
García, E.
Attie, M.
author_sort Donato, H.
title Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
title_short Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
title_full Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
title_fullStr Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
title_full_unstemmed Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis
title_sort hereditary spherocytosis. review. part i. history, demographics, pathogenesis, and diagnosis
url http://hdl.handle.net/20.500.12110/paper_03250075_v113_n1_p69_Donato
work_keys_str_mv AT donatoh hereditaryspherocytosisreviewpartihistorydemographicspathogenesisanddiagnosis
AT crisprl hereditaryspherocytosisreviewpartihistorydemographicspathogenesisanddiagnosis
AT rapettimc hereditaryspherocytosisreviewpartihistorydemographicspathogenesisanddiagnosis
AT garciae hereditaryspherocytosisreviewpartihistorydemographicspathogenesisanddiagnosis
AT attiem hereditaryspherocytosisreviewpartihistorydemographicspathogenesisanddiagnosis
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