Chromosome 9 may play a role in the development of all forms of MND and FTD
A study, led by Prof Ammar Al-Chalabi – an MND Association funded researcher, at King’s College London has found a region of DNA within chromosome 9 that contains three genes may be associated with the randomly occurring sporadic form of MND; a condition called ‘fronto-temporal dementia’ (FTD) that affects behaviour, emotional response and language skills; as well as a rare inherited form of MND called MND-FTD.
The results were published in the prestigious journal Lancet Neurologyon 31 August 2010. Prof. Orla Hardiman among many others is co-author.
Read more
Read more


The Irish MND research group has been active for 15 years and during this time has made many contributions to the understanding of Motor Neurone Disease (MND). (MND) / Amyotrophic Lateral Sclerosis (ALS) is a progressive and incurable neurological disorder that leads to muscle weakness and wasting. Currently there is no known cure.
