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Hope and help for those touched by Pallister-Killian Syndrome PKS is a rare tetrasomy of 12p. Visit www.pkskids.com for more information. To educate the medical community and promote research to ensure the early diagnosis of children with Pallister-Killian Syndrome, and to provide emotional, medical and other resources and support to familie of children with Pallister-Killian Sydrome.
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HOME ABOUT US ABOUT PKS EVENTS FOR FAMILIES NEWS SUPPORT CONTACT More Education Awareness Support Our Goal Vision Commitment Register Help Make Change Volunteer Participate or Donate Latest News Showing their love PKS Clinics at CHOP PKS Kids Live 2021 has been postponed RESEARCH OPPORTUNITY. CHOP is doing a prenatal PKS study. A hero is an ordinary individual who finds the strength to persevere and endure in spite of overwhelming obstacles. Christopher Reeve SupportUs Education Awareness Support PKS Kids provides hope and help to families.

Birth Defects, Genetic Diseases Birth Defects, Genetic Diseases Research
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