Advancing precision therapies for NAA15-related neurodevelopmental disorders

An ultra-rare genetic condition affecting global development.

Our mission is to accelerate a treatment pathway for GG and others like her.

Mom Blog
GG + NAA15
Scientific Overview
Support the Research
Therapeutic Strategy

Sweet Geej experiences seizures, movement challenges, extremely limited speech, sensory processing disorder, and motor impairment, alongside complex immune & gastrointestinal disorders. Her care involves a dedicated team of specialists across neurology, genomics, cardiology, immunology, gastroenterology, & metabolic medicine, & includes biologic and nutritional therapies that have led to minor improvements in her health and quality of life. Despite these challenges, she continues to make steady gains through intensive therapies, and the hope that one day her condition will be cured. Her journey underscores both the urgency and the promise of advancing research for children like her.

Let's advance precision therapeutics together.

At just six years old, this brave young girl lives with a rare genetic condition caused by a pathogenic NAA15 mutation.

GG’s Story -
A Sweet Geej Initiative