Pallister-Killian Syndrome - Children's Hospital of Philadelphia
Pallister-Killian syndrome (PKS) is an extremely rare genetic disorder that is present at birth. The prevalence has been estimated to be 1 in 20,000; however, it is likely that PKS is underdiagnosed …
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What is PKS? - PKSkids
What is PKS? Pallister-Killian Mosaic Syndrome or PKS is a chromosome abnormality when a tetrasomy of the short arm of chromosome 12 (12p) occurs for no known reason.