Episode notes
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 Case
Report” by Shravan Kumar Katam et al., published in the Annals of Genetics and Genetic
Disorders (November 2021). The case involves a neonate with a unique chromosomal
duplication. We discuss the clinical presentation and genetic insights for managing rare
congenital 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 complex
conditions.
Article link 🔗 https://www.remedypublications.com/annals-of-genetics-genetic-disorders-abstract.php?aid=8252
Keywords
Genomic journey's