PKS is a rare chromosomal disorder. PKS Foundation of Australia is a not for profit organisation aimed at generating awareness about the disorder within the general community and medical professionals; supporting kids and families of those affected by PKS achieve a better quality of life, through therapy and equipment support and generating sufficient resources to fund research into many of unknown facets of this disorder.
To make a secure online donation, please click on the “Make a Donation” image below.
Pallister-Killian Syndrome Foundation of Australia website is currently being upgraded
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