Inborn error of metabolism (IEM) is a spectrum of diseases that can affect the normal metabolism in children, said doctors. Screening of newborns or screening of parents during the pre-natal...
The High Court of Karnataka on Friday passed an interim order to shift a toddler afflicted with Spinal Muscular Atrophy (SMA) Type 1, a rare disease, to the Indira Gandhi...
In an exclusive interaction with BW Health care world, Subhamoy Dastidar, Co-Founder & Director, Lilac Insights, speaks about the firm and more. Excerpts: Tell us about the recent trends in...
Aimed at raising money for treatment of rare diseases that need expensive and life-long treatment and affect a small percentage of the population News:- 1)Platform launched on August...
We appreciate the kind assistance of Ms.Shruti Mohanty, Ms.Tulisa Samantaray, and Ms.Ushneet Chhabra, MSc BMG, VIT, Vellore for the posters on SATB2 Associated Syndrome Awareness...
We acknowledge the kind assistance of Ms. Poorva Samdani,Ms. Vaishnavi. R, MSc. BMG, VIT, Vellore for the poster on Smith Kingsmore Syndrome Awareness...
We acknowledge the kind assistance of Ms. Anandi Shivaram and Ms. Panchami P, MSc. BMG, VIT, Vellore for the poster of Severe Myalgic Encephalomyelitis Awareness...
8th August is celebrated as the #Chromosome8p day, a rare chromosomal disorder caused by deletion of a part of chromosome 8. Let’s join hands in spreading awareness about this disorder...
PARIS – August 6, 2021 – The U.S. Food and Drug Administration (FDA) has approved Nexviazyme® (avalglucosidase alfa-ngpt) for the treatment of patients one year of age and older with late-onset Pompe disease, a progressive...
