When his daughter, Meredith Huml, was diagnosed — finally — with facioscapulohumeral (FSHD) muscular dystrophy in 2004, Raymond Huml immediately jumped into action, researching everything he could about the disease and reaching...
आज लोक सभा में लाईलाज बीमारी मस्कुलर एट्रोफी व डिस्ट्राफी से झुंझ रहे बीमार बच्चो व वयस्को की समस्या व उनके इलाज की मांग को लेकर मामला उठाया,स्पाइन मस्कुलर एट्रोफी...
https://youtu.be/VOCwHi0p9OM Link For The Original Video:-...
GUWAHATI: A complicated and rare bicuspid aortic valve surgery on a 41-year old woman of the state was successfully carried out recently at GNRC Hospitals here, which is the first...
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...
