SKS – Smith-Kingsmore Syndrome Foundation
What is Smith-Kingsmore Syndrome? Smith-Kingsmore syndrome (SKS) is a mutation of the mTOR gene that stops the brain from developing and functioning properly, leading to …
SKS Overview - Smith-Kingsmore
Smith-Kingsmore syndrome (SKS) is a mutation of the mTOR gene that stops the brain from developing and functioning properly, leading to intellectual, developmental, behavioral and …
WHAT IS SMITH-KINGSMORE SYNDROME? Smith-Kingsmore syndrome (SKS) is a rare neurodevelopmental genetic disorder, identified in 2013, caused by changes (disease-causing …
Family & Medical Provider Guide – SKS
To help our community, the Smith-Kingsmore Syndrome Foundation, in collaboration with the SKS Medical and Scientific Advisory team, have put together a guide that can be downloaded …
Common Features Of SKS - Smith-Kingsmore
A printable and downloadable guide to Smith-Kingsmore Syndrome, that you can share with medical providers, teachers and family, can be found here in 23 languages.
Le syndrome de Smith-Kingsmore (SKS) est une maladie génétique neurodéveloppementale rare, identifiée en 2013, provoquée par des modifications ou mutations (variants pathogènes) du …
Welcome to our community – SKS - Smith-Kingsmore
Receiving a diagnosis of Smith-Kingsmore syndrome can be an overwhelming experience. There are many uncertainties that we have to deal with, today and in the future. But you’re never …
WAS IST DAS SMITH-KINGSMORE-SYNDROM? Das Smith-Kingsmore-Syndrom (SKS) ist eine seltene neurologische Entwicklungsstörung, die im Jahr 2013 identifiziert wurde und durch …
SKS RESEARCH - Smith-Kingsmore
The Smith-Kingsmore Syndrome Foundation is the only non-profit that specifically funds Smith-Kingsmore syndrome research. Our first grant was awarded to the lab of Dr Andrew Liu, in the …
What is SKS - Smith-Kingsmore
Dr. Laurie Smith, who first documented Smith-Kingsmore syndrome, talks about SKS and answers questions from our families.