Nonsense mutations are a causal factor of nearly 10% of genetic disorders. To make sense out of these nonsense mutations, we have Dr. Sandeep Eswarappa joining us in our ORDI...
What are the indications for the requirement of home ventilation? How do we go about it? Join us as Dr. Ilin Kinimi walks us through home ventilation in children through...
With adequate information, you can reduce the burden of MS with early diagnosis and treatment. Join us as Dr. Arvind Sharma walks us through Stream to deal with MS, Early...
With adequate information, it is possible to distinguish between Autism and Fragile X.Dr. Samir Hasan Dalwai & Shalini Kedia walk us through The invisible link between Autism & Fragile X...
Genetic Testing and Counseling should go hand in hand with a meticulous Clinical examination of inherited diseases, explains Prof Nalini. To know more, join us as Dr. Nalini Atchayaram explains...
Integrating metabolic biomarkers at the proteomic level will aid rare disease therapeutic research. Dr. Aditi Bhattacharya explains this, with reference to rare neurogenetic diseases through the ORDI Care For Rare...
Lysosomal storage disorders are easily mistaken for metabolic disorders thus increasing the time taken for timely diagnosis. The first step to Identify Lysosomal Storage Disorders is by proper screening. To...
It’s easy to forget your strength and who you truly are because of the world we live in. Lets us learn with Ms. Arouba Kabir an experienced counsellor & cystic...
Often NICU sick babies are treated for sepsis and other more common problems, however, more than often the clinical presentation can be disguised as a more grave problem of metabolic...
Epilepsy in children is a neurological disorder with significant psychosocial burden to families. In a country like India, huge treatment gap, education and stigma needs a well established approach for...
