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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Publicado: 2015
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03250075_v113_n1_p69_Donato
http://hdl.handle.net/20.500.12110/paper_03250075_v113_n1_p69_Donato
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spelling paper:paper_03250075_v113_n1_p69_Donato2023-06-08T15:32:00Z Hereditary spherocytosis. Review. Part I. History, demographics, pathogenesis, and diagnosis 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. 2015 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03250075_v113_n1_p69_Donato 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
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.
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
publishDate 2015
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03250075_v113_n1_p69_Donato
http://hdl.handle.net/20.500.12110/paper_03250075_v113_n1_p69_Donato
_version_ 1768542739257884672