Labroots

New Test for Rare Neurological Disease Recommended for Kids with Symptoms

There is now a blood test that can diagnose a rare neurometabolic condition known as Glut1 deficiency syndrome, or De Vivo disease. Glut1 deficiency syndrome is caused by a mutation in a gene called ...
Business Wire

Invitae Announces Major Expansion of Its Test Menu for Neurological, Pediatric, and Rare Genetic Conditions and Introduces New Panels for Inherited Metabolic Disorders and ...

SAN FRANCISCO--(BUSINESS WIRE)--Invitae Corporation (NYSE:NVTA), a genetic information company, today announced that it has expanded its genetic testing offering with hundreds of additional genes and ...

Newborn screening in Texas expands to include rare neurological condition

The Texas Department of State Health Services (DSHS) announced on Tuesday that an additional test for a rare neurological ...
Business Insider

Baylor Genetics to Showcase the Expanding Role and Clinical Value of Genetic Testing in Pediatric Neurology at the 2025 Child Neurology Society Annual Meeting

HOUSTON, Sept. 22, 2025 (GLOBE NEWSWIRE) -- Baylor Genetics, a clinical diagnostic laboratory at the forefront of genetic testing, today announced it will showcase its leadership in pediatric ...