Epidemiology of inherited metabolic disorders in newborn screening: insights from three years of experience in Southern Iran

Epidemiology of inherited metabolic disorders in newborn screening: insights from three years of experience in Southern Iran

Abstract Background Newborn screening is essential for the early detection of congenital genetic and metabolic disorders, enabling timely intervention to prevent morbidity, mortality, and disabilities associated with inherited metabolic disorders (IMDs). The Iranian Neonatal Screening Program pilote...

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Main Authors: Leila Salarian, Homa Ilkhanipoor, Anis Amirhakimi, Zhila Afshar, Saman Nahid, Fariba Moradi Ardekani, Nazila Rahimi, Negar Yazdani, Abdolhossein Nikravesh, Zahra Beyzaei, Hossein Moravej
Format: Article
Language:English
Published: BMC 2025-02-01
Series:Orphanet Journal of Rare Diseases
Subjects:
Metabolism
Inborn errors of metabolism
Neonatal screening
Genetic diseases
Inherited metabolic disease
Dried blood spots
Online Access:https://doi.org/10.1186/s13023-025-03602-w
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https://doi.org/10.1186/s13023-025-03602-w

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