PKS Kids

Education~Awareness~Support for those affected by Pallister-Killian Syndrome

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Official US Rare Disease Day Partner

 
We support the Global Genes Project.  Please click on the logo above to see how you can raise money for PKS Kids!

Contact gpeters@pkskids.net if you have any questions.  

 

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TM

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 Mission Statement
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.

 

 

 

 

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