ReviewWorld journal of clinical pediatrics2024
Genetic variation features of neonatal hyperbilirubinemia caused by inherited diseases.
Review in World journal of clinical pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
backgroundGenetic factors play an important role in neonatal hyperbilirubinemia (NH) caused by genetic diseases.
aimTo explore the characteristics of genetic mutations associated with NH and analyze the correlation with genetic diseases.
methodsThis was a retrospective cohort study. One hundred and five newborn patients diagnosed with NH caused by genetic diseases were enrolled in this study between September 2020 and June 2023 at the Second Affiliated Hospital of Xiamen Medical College. A 24-gene panel was used for gene sequencing to analyze gene mutations in patients. The data were analyzed
resultsSeventeen frequently mutated genes were found in the 105 patients.
conclusionGenetic mutations are associated with NH and significantly increase the risk of disease in affected newborns.
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