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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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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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 |