Mitchell was diagnosed with Pallister-Killian Syndrome (PKS), a rare and complex genetic condition that affects different cells in the body in unpredictable ways. With fewer than 500 known cases worldwide – and only around 30 in Australia – Mitchell is one of just a handful of children living with PKS in WA. The post Gold Series – Perth: $1.5M in rare care. appeared first on Perth Childrens Hospital Foundation.
