National Neonatology Forum (NNF) Joins Forces with Clinical Geneticists for Webinar Series

The National Neonatology Forum (NNF) and leading clinical geneticists have debuted a monthly scientific series. The initiative aims to revolutionize NICU outcomes through expert-led sessions on genomic testing, metabolic emergencies, and dysmorphology.

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In an effort to enhance specialized care for the most vulnerable patients, a new Monthly Webinar Series: Genetics & Rare Diseases for Neonatologists has been announced.

This initiative aims to equip neonatologists with the critical tools needed to identify, diagnose, and manage genetic conditions within the Neonatal Intensive Care Unit (NICU).

This educational initiative is organized by the National Neonatology Forum (NNF) in strategic collaboration with leading Clinical Geneticists.

Coordinated by Dr. Amit Upadhyay, Dr. Mayank Nilay, and Dr. Debarun, the program features a revised scientific schedule that brings together leading experts to discuss the frontiers of neonatal genetics.

Scientific Program

The webinars will be held on the 28th of every month, providing a consistent platform for professional development.

DateTopicFaculty
Feb 28, 2026Newborn Screening (NBS) for Rare DiseasesProf. (Dr.) Seema Kapoor
Mar 28, 2026Approach to the Dysmorphic Neonate in NICUDr. Veronica
Apr 28, 2026Genetic Causes of Neonatal HypotoniaDr. Ravneet
May 28, 2026Inborn Errors of Metabolism (IEM)Dr. Haseena
Jun 28, 2026Neonatal Seizures: When to Think Genetic?Dr. Rhea
Jul 28, 2026Neonatal Cholestasis: Genetic EtiologiesDr. Swasti
Aug 28, 2026Skeletal Dysplasias (SKD) in the NeonateDr. Selva
Sep 28, 2026Genetic Causes of Congenital Heart DiseaseDr. Bhawana
Oct 28, 2026Disorders of Sex Development (DSD)Dr. Sarath R S
Nov 28, 2026Rapid Genomic Testing in the NICUDr. Mayuri
Dec 28, 2026Connective Tissue & Vascular FragilityDr. Shifali Gupta
Jan 28, 2027Counseling Parents After a DiagnosisDr. Eshan

Please note that the schedule and faculty may be subject to change due to logistical reasons.

Core Learning Objectives

The series is designed to move beyond theory and into practical, bedside application. Participants will:

  • Strengthen Recognition Skills: Learn to identify red flags such as dysmorphism, metabolic instability, and unexplained seizures.
  • Master Diagnostics: Implement systematic pathways for genetic testing, including exome sequencing and microarrays.
  • Manage Emergencies: Enhance the ability to stabilize genetic crises, including salt-wasting and metabolic emergencies.
  • Integrate Genomics: Develop competence in interpreting rapid genomic reports and managing Variants of Uncertain Significance (VUS).
  • Improve Communication: Refine skills in discussing prognosis, recurrence risks, and reproductive planning with families.
  • Foster Collaboration: Build stronger links between neonatologists, geneticists, and laboratory teams for precision treatment.

Through this collaborative effort, the program seeks to ensure that every neonate with a suspected rare disease receives a timely referral and a path toward precision medicine.

Contact Information: For registration details and further inquiries, please contact the Webinar Coordinators.

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