PKS (medical condition): A rare genetic disorder due to tetrasomy of the 12th chromosome.
See also:
Pallister-Killian Syndrome:
»Introduction: Pallister-Killian Syndrome
PKS is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that PKS, or a subtype of PKS,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
PKS: Another name for Pallister-Killian Syndrome (or close medical condition association).
»Introduction: Pallister-Killian Syndrome
These medical disease topics may be related to PKS:
Source - NIH
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