CHARGE syndrome presenting with persistent hypoglycemia: case report and overview of the main genetic syndromes associated with neonatal hypoglycemia

Abstract Background CHARGE syndrome (CS) is an autosomal dominant genetic condition whose recognition in the neonatal period is complicated by considerable phenotypic variability. Pediatric patients with genetic disorders have a known high incidence of hypoglycemia, due to many concurring factors. T...

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Main Authors: Alessandra Consales (Author), Beatrice Letizia Crippa (Author), Lorenzo Colombo (Author), Roberta Villa (Author), Francesca Menni (Author), Claudia Giavoli (Author), Fabio Mosca (Author), Maria Francesca Bedeschi (Author)
Format: Book
Published: BMC, 2022-08-01T00:00:00Z.
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