TY  - GEN
AU  - Colombatti,Raffaella
AU  - Cela,Elena
AU  - Lobitz,Stephan
AU  - Elion,Jacques
TI  - Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies
SN  - books978-3-03921-615-4
PY  - 2019///
PB  - MDPI - Multidisciplinary Digital Publishing Institute
KW  - glucose-6-phosphate dehydrogenase
KW  - hydroxyurea/hydroxycarbamide
KW  - n/a
KW  - cord blood
KW  - screening
KW  - hemoglobin pattern
KW  - capillary electrophoresis
KW  - sickle cell disease
KW  - (recommended) screening panel
KW  - vaso-occlusive crisis
KW  - Guthrie spots
KW  - newborn screening)
KW  - foetal haemoglobin
KW  - harmonisation
KW  - review
KW  - birth prevalence
KW  - G6PD deficiency
KW  - prevention
KW  - end-organ damage
KW  - thalassemia
KW  - MALDI-TOF
KW  - IEF
KW  - acute chest syndrome
KW  - India
KW  - sickle cell and thalassaemia screening programme
KW  - 'Getting to Outcomes'
KW  - newborn screening
KW  - hemoglobinopathy
KW  - service users
KW  - public health engagement
KW  - automated HPLC
KW  - Kaduna State
KW  - gene therapy for haemoglobinopathies
KW  - ?-globin gene
KW  - methods
KW  - neonatal screening program
KW  - malaria
KW  - Plasmodium vivax
KW  - sub-Saharan Africa
KW  - patient organisations
KW  - health policy
KW  - pathophysiology
KW  - Sickle Cell Disease
KW  - mass spectrometry
KW  - sickle cell disorder
KW  - neonatal screening
KW  - non-tribal
KW  - Nigeria
KW  - point-of-care
KW  - HPLC
KW  - laboratory methods
KW  - registry
KW  - patient advocacy
KW  - bone marrow transplant
KW  - anaemia
KW  - hemoglobinopathies
KW  - tribal
KW  - newborn
KW  - burden of disease
KW  - patient representatives
KW  - diagnostics
KW  - policy making
KW  - haemolysis
KW  - Caribbean
KW  - high performance liquid chromatography (HPLC)
KW  - sickle cell disease (SCD)
KW  - implementation science
N1  - Open Access
N2  - 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
UR  - https://mdpi.com/books/pdfview/book/1649
UR  - https://directory.doabooks.org/handle/20.500.12854/54644
ER  -