A Rogue Gene Is Causing Seizures in Babies. Here’s How MSU Wants to Stop It
Two rare diseases caused by a malfunctioning gene that triggers seizures or involuntary movements in children as early as a few days old have left scientists searching for answers and better treatment options.
Michigan State University researchers are closer to understanding the source, a gene known as GNAO1 and the transformations it can take on, and potentially stopping its devastating effects by uncovering key differences in the way it functions.
The rogue gene, linked to epilepsy and movement disorders, is the culprit of two recently identified conditions called early infantile epileptiform encephalopathy, or EIEE17, and Neurodevelopmental Disorder with Involuntary Movements, or NEDIM.
Click here to read more.
Microsurgical Approaches to Aneurysms and Skull Base Diseases 2017
Oct. 26-28, 2017; Jacksonville, Fla.
Pituitary Tumors: Diagnostic and Treatment Dilemmas
Oct. 27, 2017; New York
GOODMAN Oral Board Preparation Course Tumor
Nov. 1-3, 2017; Glendale, Ariz.
8th World Congress of Neuroendoscopy
Nov. 1-4, 2017; Cape Town, South Africa
3rd Annual Selected Topics in Craniomaxillofacial Surgery
Nov. 4, 2017 - Nov. 5, 2017; Boston, Mass.
Be the first to reply using the above form.