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PKS KidsTM is a 501(c)3 non-profit organization aimed at helping all people involved with Pallister-Killian Syndrome. Caregivers, family members, friends, teachers and medical professionals can all find help and support here.
Our
To promote research, provide education, and raise awareness within the medical community in order to ensure early diagnoses of children with Pallister-Killian Syndrome (PKS). To provide resources and support to families, therapists and caregivers of children with PKS.
If you'd like to learn more about Pallister-Killian Syndrome click here.