Causes of MSI (Syndromes and Conditions)
Information The following two links are are good starting point National Deaf Children's Society Information for Parents 'Congenital cytomegalovirus and deafness' You need to be a member to access this information but membership is free to parents of deaf children and the professionals who work with them. National Congenital CMV Disease Registry (US) Information booklet - 'What everyone should know about CMV' More links CDC Website CMV Deafblind International CMV A - Z of Deafblindness CMV by James Gallagher The Ear Foundation run a one day CMV Focus Day. Search their website for course dates. Reduced rates for parents. Journal of Paediatric Child Health (2005) Research paper- Symptomatic infant characteristics of congenital cytomegalovirus disease in Australia Government of South Australia Information on transmission, diagnosis and management Support Groups The UK Congential CMV Association The Association is run on a voluntary basis by the parents of CMV children. They publish a regular newsletter, put families in touch with others, raise awareness and aid CMV research. Contential CMV Association (America)
Information
The following two links are are good starting point
More links
Support Groups
MSI Index