Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies
Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the International Journal of Neonatal Screening. Sickle cell disease is one of the most common inherited blood disorders, with a huge impact on health care systems due to high morbidity and high mortality a...
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| Main Authors: | , , , |
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| Format: | Online |
| Sprog: | engelsk |
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MDPI - Multidisciplinary Digital Publishing Institute
2021
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| Online adgang: | 42565 |
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| _version_ | 1869515159209246720 |
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| author | Colombatti, Raffaella Cela, Elena Lobitz, Stephan Elion, Jacques |
| author_browse | Cela, Elena Colombatti, Raffaella Elion, Jacques Lobitz, Stephan |
| author_facet | Colombatti, Raffaella Cela, Elena Lobitz, Stephan Elion, Jacques |
| author_sort | Colombatti, Raffaella |
| collection | Directory of Open Access Books |
| description | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the International Journal of Neonatal Screening. Sickle cell disease is one of the most common inherited blood disorders, with a huge impact on health care systems due to high morbidity and high mortality associated with the undiagnosed disease. Newborn screening helps to make the diagnosis early and to prevent fatal complications and diagnostic odysseys. This book gives an overview of diagnostic standards in newborn screening for sickle cell disease and examples of existing newborn screening programs. |
| format | Online |
| id | doab-20.500.12854ir-54644 |
| institution | Directory of Open Access Books |
| language | eng |
| publishDate | 2021 |
| publishDateRange | 2021 |
| publishDateSort | 2021 |
| publisher | MDPI - Multidisciplinary Digital Publishing Institute |
| publisherStr | MDPI - Multidisciplinary Digital Publishing Institute |
| record_format | ojs |
| spelling | doab-20.500.12854ir-546442024-04-05T12:38:46Z Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies Colombatti, Raffaella Cela, Elena Lobitz, Stephan Elion, Jacques QD1-999 Q1-390 glucose-6-phosphate dehydrogenase hydroxyurea/hydroxycarbamide n/a cord blood screening hemoglobin pattern capillary electrophoresis sickle cell disease (recommended) screening panel vaso-occlusive crisis Guthrie spots newborn screening) foetal haemoglobin harmonisation review birth prevalence G6PD deficiency prevention end-organ damage thalassemia MALDI-TOF IEF acute chest syndrome India sickle cell and thalassaemia screening programme ‘Getting to Outcomes’ newborn screening hemoglobinopathy service users public health engagement automated HPLC Kaduna State gene therapy for haemoglobinopathies ?-globin gene methods neonatal screening program malaria Plasmodium vivax sub-Saharan Africa patient organisations health policy pathophysiology Sickle Cell Disease mass spectrometry sickle cell disorder neonatal screening non-tribal Nigeria point-of-care HPLC laboratory methods registry patient advocacy bone marrow transplant anaemia hemoglobinopathies tribal newborn burden of disease patient representatives diagnostics policy making haemolysis Caribbean high performance liquid chromatography (HPLC) sickle cell disease (SCD) implementation science thema EDItEUR::P Mathematics and Science::PN Chemistry Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies is a Special Issue of the International Journal of Neonatal Screening. Sickle cell disease is one of the most common inherited blood disorders, with a huge impact on health care systems due to high morbidity and high mortality associated with the undiagnosed disease. Newborn screening helps to make the diagnosis early and to prevent fatal complications and diagnostic odysseys. This book gives an overview of diagnostic standards in newborn screening for sickle cell disease and examples of existing newborn screening programs. 2021-02-11T20:59:31Z 2021-02-11T20:59:31Z 2019-12-09 11:49:15 2019 book 42565 9783039216154 9783039216147 https://directory.doabooks.org/handle/20.500.12854/54644 eng application/octet-stream Attribution-NonCommercial-NoDerivatives 4.0 International https://mdpi.com/books/pdfview/book/1649 MDPI - Multidisciplinary Digital Publishing Institute 10.3390/books978-3-03921-615-4 10.3390/books978-3-03921-615-4 46cabcaa-dd94-4bfe-87b4-55023c1b36d0 9783039216154 9783039216147 162 open access |
| spellingShingle | QD1-999 Q1-390 glucose-6-phosphate dehydrogenase hydroxyurea/hydroxycarbamide n/a cord blood screening hemoglobin pattern capillary electrophoresis sickle cell disease (recommended) screening panel vaso-occlusive crisis Guthrie spots newborn screening) foetal haemoglobin harmonisation review birth prevalence G6PD deficiency prevention end-organ damage thalassemia MALDI-TOF IEF acute chest syndrome India sickle cell and thalassaemia screening programme ‘Getting to Outcomes’ newborn screening hemoglobinopathy service users public health engagement automated HPLC Kaduna State gene therapy for haemoglobinopathies ?-globin gene methods neonatal screening program malaria Plasmodium vivax sub-Saharan Africa patient organisations health policy pathophysiology Sickle Cell Disease mass spectrometry sickle cell disorder neonatal screening non-tribal Nigeria point-of-care HPLC laboratory methods registry patient advocacy bone marrow transplant anaemia hemoglobinopathies tribal newborn burden of disease patient representatives diagnostics policy making haemolysis Caribbean high performance liquid chromatography (HPLC) sickle cell disease (SCD) implementation science thema EDItEUR::P Mathematics and Science::PN Chemistry Colombatti, Raffaella Cela, Elena Lobitz, Stephan Elion, Jacques Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
| title | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
| title_full | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
| title_fullStr | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
| title_full_unstemmed | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
| title_short | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
| title_sort | newborn screening for sickle cell disease and other haemoglobinopathies |
| topic | QD1-999 Q1-390 glucose-6-phosphate dehydrogenase hydroxyurea/hydroxycarbamide n/a cord blood screening hemoglobin pattern capillary electrophoresis sickle cell disease (recommended) screening panel vaso-occlusive crisis Guthrie spots newborn screening) foetal haemoglobin harmonisation review birth prevalence G6PD deficiency prevention end-organ damage thalassemia MALDI-TOF IEF acute chest syndrome India sickle cell and thalassaemia screening programme ‘Getting to Outcomes’ newborn screening hemoglobinopathy service users public health engagement automated HPLC Kaduna State gene therapy for haemoglobinopathies ?-globin gene methods neonatal screening program malaria Plasmodium vivax sub-Saharan Africa patient organisations health policy pathophysiology Sickle Cell Disease mass spectrometry sickle cell disorder neonatal screening non-tribal Nigeria point-of-care HPLC laboratory methods registry patient advocacy bone marrow transplant anaemia hemoglobinopathies tribal newborn burden of disease patient representatives diagnostics policy making haemolysis Caribbean high performance liquid chromatography (HPLC) sickle cell disease (SCD) implementation science thema EDItEUR::P Mathematics and Science::PN Chemistry |
| topic_facet | QD1-999 Q1-390 glucose-6-phosphate dehydrogenase hydroxyurea/hydroxycarbamide n/a cord blood screening hemoglobin pattern capillary electrophoresis sickle cell disease (recommended) screening panel vaso-occlusive crisis Guthrie spots newborn screening) foetal haemoglobin harmonisation review birth prevalence G6PD deficiency prevention end-organ damage thalassemia MALDI-TOF IEF acute chest syndrome India sickle cell and thalassaemia screening programme ‘Getting to Outcomes’ newborn screening hemoglobinopathy service users public health engagement automated HPLC Kaduna State gene therapy for haemoglobinopathies ?-globin gene methods neonatal screening program malaria Plasmodium vivax sub-Saharan Africa patient organisations health policy pathophysiology Sickle Cell Disease mass spectrometry sickle cell disorder neonatal screening non-tribal Nigeria point-of-care HPLC laboratory methods registry patient advocacy bone marrow transplant anaemia hemoglobinopathies tribal newborn burden of disease patient representatives diagnostics policy making haemolysis Caribbean high performance liquid chromatography (HPLC) sickle cell disease (SCD) implementation science thema EDItEUR::P Mathematics and Science::PN Chemistry |
| url | 42565 |
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