Turner's syndrome is a sporadic disorder of human females in which all
or part of one X chromosome is deleted(1). Intelligence is usually no
rmal(2) but social adjustment problems are common(3). Here we report a
study of 80 females with Turner's syndrome and a single X chromosome,
in 55 of which the X was maternally derived (45,X-m) and in 25 it was
of paternal origin (45,X-p). Members of the 45,XP group were signific
antly better adjusted, with superior verbal and higher-order executive
function skills, which mediate social interactions(4). Our observatio
ns suggest that there is a genetic locus for social cognition, which i
s imprinted(5) and is not expressed from the maternally derived X chro
mosome. Neuropsychological and molecular investigations of eight femal
es with partial deletions of the short arm of the X chromosome(6) indi
cate that the putative imprinted locus escapes inactivation(7), and pr
obably lies on Xq or close to the centromere on Xp. If expressed only
from the X chromosome of paternal origin, the existence of this locus
could explain why 46,XY males (whose single X chromosome is maternal)
are more vulnerable to developmental disorders of language and social
cognition, such as autism, than are 46,XX females(8).