Tetrasomy 12p

MONDO:0011146

Pallister-Killian syndrome (PKS) is a rare multiple congenital anomaly/intellectual deficit syndrome caused by mosaic tissue-limited tetrasomy for chromosome 12p.

Also known as: Isochromosome 12p mosaicism, Isochromosome 12p syndrome, Pallister Killian Mosaic Syndrome, Pallister-Killian syndrome, Pallister-Killian syndrome, Somatic mosaicism, tetrasomy type 12p, Hexasomy 12P, Mosaic, Isochromosome 12P syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Tetrasomy 12p itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic disease (7133) ↑ Overgrowth syndrome (49) ↑ Partial trisomy/tetrasomy of the short arm of chromosome 12 (0)

Including sub-types (0) Tagged with Tetrasomy 12p (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.