Welcome to Ped Mind Institute,
Human genom include 3.1 Milliards paired bases in a simple chromosom set. To date, there are known more than 6100 rare genetic diseases in human being, whereas 70 % of them are found exclusively in children. Nearly 15 % of all children treated in intensive care units have a rare genetic disease. The diagnosis of a rare genetic disease is difficult due to the variability of the diseases.
Ped Mind Institute focus on innovative research in rare genetic diseases in children.
Ped Mind Institute was established in 2010 to take care for children, who have born with a rare genetic disease or syndrome like Allan-Herndon Dudley syndrome, Hutchinson-Gilford syndrome, Kawasaki disease and others.
Since 2010, we spend enormous engagement in genetic rare diseases in pediatric patients and established scientific cooperations all over the world.
We aim to find innovative genetic therapies and targets for treatment and follow innovative new aspects of research.
It is incredible what a tiny mutation or change in a child's DNA can have lasting and serious consequences for the child's health.
The best for our children.
Best wishes,
Prof. Stefan Bittmann M.A.
Professor for Pediatrics
Head of Department of Pediatrics and Ped Mind institute (PMI)
Visiting Professor, Faculty of Medicine, Shangluo Vocational and Technical College (SVTC), Shangluo, China
