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Autore: | Colombatti Raffaella |
Titolo: | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
Pubblicazione: | MDPI - Multidisciplinary Digital Publishing Institute, 2019 |
Descrizione fisica: | 1 electronic resource (162 p.) |
Soggetto non controllato: | glucose-6-phosphate dehydrogenase |
hydroxyurea/hydroxycarbamide | |
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 | |
Persona (resp. second.): | CelaElena |
LobitzStephan | |
ElionJacques | |
Sommario/riassunto: | 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. |
Titolo autorizzato: | Newborn Screening for Sickle Cell Disease and other Haemoglobinopathies |
ISBN: | 3-03921-615-5 |
Formato: | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione: | Inglese |
Record Nr.: | 9910367754603321 |
Lo trovi qui: | Univ. Federico II |
Opac: | Controlla la disponibilità qui |