Wl. Yan et al., CHROMOSOME 22Q11.2 INTERSTITIAL DELETIONS AMONG CHILDHOOD-ONSET SCHIZOPHRENICS AND MULTIDIMENSIONALLY IMPAIRED, American journal of medical genetics, 81(1), 1998, pp. 41-43
Since its first description almost a century ago schizophrenia with ch
ildhood onset, a rare yet devastating disorder, has been diagnosed in
children as young as age 5, Recently, the velocardiofacial syndrome, w
hose underlying cause is interstitial deletions of 22q11.2, was found
in 2 of 100 cases of schizophrenics with adult onset [Karayiorgou et a
l., Proc Natl Acad Sci USA 92:7612-7616, 1995]. No study has documente
d the prevalence of velocardiofacial syndrome and the 22q11.2 deletion
in a population of schizophrenics with childhood onset, Here we descr
ibe the result of such a study in a sample originally selected for a t
rial of atypical antipsychotic drugs, A separate group of patients was
also included in the study; they can best be accounted for as a varia
nt of childhood-onset schizophrenia (COS) and had been provisionally t
ermed ''multidimensionally impaired.'' Fluorescent in situ hybridizati
on screening of 32 COS and 21 multidimensionally impaired patients rev
ealed 1 COS patient with an interstitial deletion spanning at least 2.
5 megabases. (C) 1998 Wiley-Liss, Inc.