Neonatal screening programs are essential for early identification and management of congenital disorders, metabolic conditions, and genetic diseases in newborns. Early diagnosis and intervention can prevent severe health outcomes, including developmental delays, disabilities, or even death (Akinmoladun et al., 2023). In Nigeria, neonatal screening programs are not yet universally implemented, and many newborns, especially in rural areas like Niger State, are not screened for critical conditions such as sickle cell disease, phenylketonuria, and hypothyroidism.
In Niger State, the implementation of neonatal screening programs has been limited, with challenges including lack of awareness, insufficient healthcare infrastructure, and resource constraints. This study will investigate the effectiveness of neonatal screening programs in Niger State, examining their ability to detect and address early childhood health issues.
Despite the potential benefits of neonatal screening, the implementation and effectiveness of such programs in Niger State remain underexplored. Many infants miss early diagnoses of preventable conditions, which can lead to lifelong disabilities or death. There is a need to evaluate the effectiveness of existing neonatal screening programs and recommend strategies for improving early diagnosis and intervention.
The study will focus on neonatal screening programs in Niger State, examining both urban and rural healthcare settings. Data will be collected from hospitals and healthcare providers offering screening services. Limitations include potential biases in reporting and logistical challenges in reaching remote areas.
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