#68 The Hidden Danger in Newborns: OTC Deficiency Explained by a Geneticist and a Mother
In this episode of It Happened To Me, we share a story of love, loss, and advocacy in the rare disease community.
We are joined by Jordan Kruse, whose son, Pruitt, was born with ornithine transcarbamylase (OTC) deficiency, and Dr. Susan Berry, a geneticist at M Health Fairview and professor at the University of Minnesota Medical School, who specializes in rare metabolic disorders like OTC deficiency and helped Pruitt.
OTC deficiency is a rare urea cycle disorder (UCD) that prevents the body from properly removing ammonia from the blood. This dangerous buildup can cause severe complications, and in Pruitt’s case, tragically ended his life at only six months old.
Through her grief, Jordan founded The Brave Little One Foundation, honoring Pruitt’s legacy by supporting families facing medical hardship and raising awareness about rare genetic conditions. Together, she and Dr. Berry shed light on:
What OTC deficiency is and how it affects the body
Why newborn screening doesn’t always catch the condition
The role of geneticists and medications in diagnosing and managing OTC deficiency
Jordan’s experience advocating for Pruitt’s care in a complex medical system
The importance of foundations and rare disease organizations in offering resources and hope
What families and healthcare providers need to know about navigating rare disease diagnoses
Resources:
The Rare Diseases Clinical Research Network (RDCRN Consortia)
Ornithine transcarbamylase deficiency explained by MedlinePlus
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