Feb 25, 2026

Cracking the Code: How Genetics Is Rewriting Neonatal Medicine
Dr. Jeffrey Whitsett reflects on five decades in neonatal care, tracing the evolution from limited support for preemies to today’s cutting-edge genetic discoveries. Discover how rare gene mutations like TBX4 are reshaping our understanding of lung...
Feb 24, 2026
Cracking the
Code: How Genetics Is Rewriting Neonatal Medicine
Dr. Jeffrey
Whitsett reflects on five decades in neonatal care, tracing the
evolution from limited support for preemies to today’s cutting-edge
genetic discoveries. Discover how rare gene mutations like TBX4 are
reshaping our understanding of lung...
Feb 18, 2026

From Knee Pain to Gene Discovery: One Family’s Unexpected Diagnosis
What started as routine investigations into hereditary knee problems turned into a life-altering discovery for Luke Stockdale and his family — a TBX4 gene mutation linked to pulmonary arterial hypertension (PAH). In this episode, Luke shares...
Feb 17, 2026
From Knee Pain to Gene Discovery: One Family’s Unexpected Diagnosis
What started as routine investigations into hereditary knee problems turned into a life-altering discovery for Luke Stockdale and his family — a TBX4 gene mutation linked to pulmonary arterial hypertension (PAH). In this episode, Luke shares how...
Feb 11, 2026

How a Global Team Is Rewriting the
TBX4 Playbook
Rare diseases thrive in isolation. TBX4Life is changing that.
In this episode, Drs. Prapa and Danhaive share how
international collaboration is creating real-time change for
patients. From newborn screening to natural history studies to
rethinking how we talk about...