Episode 1 description: In this episode, we explore a rare genetic condition from the article“Atypical Features in a Neonate with de novo 17p11.2p13.2 Duplication Syndrome - A CaseReport” by Shravan Kumar Katam et al., published in the Annals of Genetics and GeneticDisorders (November 2021). The case involves a neonate with a unique chromosomalduplication. We discuss the clinical presentation and genetic insights for managing rarecongenital disorders. Tune in to learn how advances in genetics are transforming neonatal care.Listeners will gain valuable insights into the role of genetic research in diagnosing complexconditions.Article link 🔗 https://www.remedypublications.com/annals-of-genetics-genetic-disorders-abstract.php?aid=8252

Ver todos los episodios