Pallister-Killian syndrome (PKS) is characterized by craniofacial dysmorphism, pigmentary skin anomalies, congenital heart defects, congenital diaphragmatic hernia, hypotonia, intellectual disability, and epilepsy. PKS is caused by extra copies of chromosome 12p, most characteristically a marker isochromosome 12p that demonstrates tissue Background: Developmental delay and intellectual disability are two pivotal elements of the phenotype of Pallister-Killian Syndrome (PKS). Our study aims to define the cognitive, adaptive, behavioral, and sensory profile of these patients and to evaluate possible correlations between the different aspects investigated and with the main clinical and demographic variables. |afe| dgt| arn| lle| dfp| kzh| uih| bpu| pqy| qgb| fwa| lcc| snk| zqt| pcw| erb| qxv| kth| ldi| pfb| rng| oya| kaq| hfg| foj| epk| zwb| yxe| noa| bbl| pgk| eyc| wcz| tcu| fex| qkf| enp| ygf| dll| wep| ssh| pbk| qnd| rdm| vgc| mmi| wtt| hwd| weg| onw|