These guidelines have been developed by a committee consisting of representatives of clinical genetic services, genetic testing laboratories, the CJD Support Group Network (CJDSGN) and the Australian National Creutzfeldt-Jakob Disease Registry (ANCJDR). Feedback and information from the New Zealand CJD Register, Human Genetics Society of Australasia and Genetic Services is incorporated.
www1.racgp.org.au
Although rare, Creutzfeldt–Jakob disease is always fatal. General practitioners are often the first to see the patient, so ongoing awareness of the disease is essential.
CJD Awareness T-Shirt – CJD Support Group Network Australia
www.cjdsupport.org.au
With a front print designed to raise awareness for CJD and the back reads ‘Support for all Australians affected by prion disease, CJD FFI GSS’ plus contact information for the CJDSGN. The left sle...
Run 4 CJD 2024 – CJD Support Group Network Australia
www.cjdsupport.org.au
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15th Annual National CJD Conference – CJD Support Group Network Australia
www.cjdsupport.org.au
© 2024 CJD Support Group Network Australia. The CJDSGN acknowledges the funding provided by the Department of Health that assists towards the cost of this website. Disclaimer Privacy Policy© 2024 CJD Support Group Network Australia.
The CJDSGN acknowledges the funding provided by the Department of Health
that assists towards the cost of this website.
Disclaimer Privacy Policy
