The initiative could speed up diagnoses for rare genetic conditions that affect thousands of children every year. View on ...

Author: Dr Shrikant Jamdade, Clinical Geneticist, Mumbai Spinal Muscular Atrophy (SMA) is a common genetic disorder affecting ...

Inaccurate naming of genetic diseases is resulting in some rare genetic diseases needlessly being undiagnosed, University of ...

After a seven-year search for answers, a family from Eden, Utah, has received a life-changing diagnosis for their daughter ...

An Overland Park teen completed a 150-mile bike journey Sunday to raise awareness and hope for his rare genetic disorder.

A mother is “absolutely broken” following the death of her two-year-old daughter from a rare genetic condition that also ...

The U.S. Food and Drug Administration approved IntraBio's drug for a rare and fatal genetic disorder, the health regulator ...

Now, at two years old, Mirlee Janice Ramirez and her beautiful smile show how far they've come since KENS 5's Sarah Forgany ...

This discovery is not only a breakthrough in understanding brain disorders, but also highlights the rising influence of ...

The U.S. Food and Drug Administration approved Zevra Therapeutics' drug for a rare and fatal genetic disorder, making it the ...

The Khyber Pakhtunkhwa (KP) government is considering offering free treatment for patients with Spinal Muscular Atrophy (SMA) ...

Shares of Biohaven climbed 13% premarket on Monday after the biotech company said its treatment for a rare neurological ...