Brief report: Association of sex chromosome anomalies with childhood- onset psychotic disorders

Journal of the American Academy of Child and Adolescent Psychiatry

Volumn 37, Issue 3, 1998, Pages 292-296

  Kumra, Sanjiv ^a   Wiggs, Edythe ^a   Krasnewich, Donna ^a   Meck, Jeanne ^a   Smith, Ann C M ^b   Bedwell, Jeffrey ^a   Fernandez, Thomas ^a   Jacobsen, Leslie K ^a   Lenane, Marge ^a   Rapoport, Judith L ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b Building 10 ^*

Author keywords

Childhood onset psychotic disorders; Neurodevelopmental impairments; Sex chromosome anomalies

Indexed keywords

CLOZAPINE;

ADOLESCENT; ADULT; ANEUPLOIDY; ARTICLE; CHILD; CYTOGENETICS; FEMALE; GENETIC PREDISPOSITION; HUMAN; HUMAN CELL; INCIDENCE; KARYOTYPE; KARYOTYPE 47,XXY; KARYOTYPE 47,XYY; MAJOR CLINICAL STUDY; MALE; MOSAICISM; PRIORITY JOURNAL; PSYCHOSIS; SCHIZOPHRENIA; SEX CHROMOSOME ABERRATION;

EID: 0031937498     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-199803000-00014     Document Type: Article

References (22)

1. Alaghband-Rad J, Kumra S, Lenane MC et al. (1998), Early-onset schizophrenia: mental retardation in siblings (letter). J Am Acad Child Adolesc Psychiatry 37:137-138
2. Alaghband-Rad J, McKenna K, Gordon C e, al. (1995), Childhood-onset schizophrenia: the severity of premorbid course. J Am Acad Child Adolesc Psychiatry 34:1273-1283
3. Bender BG, Linden MG, Robinson A (1989), Verbal and spatial processing efficiency in 32 children with sex chromosome abnormalities. Pediatr Res 25:577-579
4. Bender BG, Linden MG, Robinson A (1996), Environment and developmental risk in children with sex chromosome abnormalities. J Am Acad Child Adolesc Psychiatry 26:499-503
5. Crow TJ (1993), Sexual selection, Machiavellian intelligence, and the origins of psychosis. Lancet 342:594-598
6. DeLisi LE, Friedrich U, Wahlstrom J et al. (1994), Schizophrenia and sex chromosome anomalies. Schizophr Bull 20:495-505
7. Franke P, Maier W, Halutzinger M, Weiffenbach O (1996), Fragile-X carrier females: evidence for a distinct psychopathological phenotype? Am J Med Genet 64:334-339
8. Gordon CT, Krasnewich D, White B, Lenane M, Rapoport JL (1994), Brief report: translocation involving chromosomes 1 and 7 in a boy with childhood-onset schizophrenia. J Autism Dev Disord 24:537-545
9. Gustavson KH, Holmgren G, Blomqiust K (1987), Chromosomal aberrations in mildly mentally retarded children in a northern Swedish county. Ups J Med Sci Suppl 44:165-168
10. Hodes ME, Dlouhy SR (1996), The proteolipid protein gene: double, double . . . and trouble. Am J Hum Genet 59:12-15
11. Kumra S, Jacobsen LK, Lenane M et al. (1998), "Multidimensionally impaired disorder": is it a variant of very early-onset schizophrenia? J Am Acad Child Adolesc Psychiatry 37:91-99
12. McKenna K, Gordon C, Lenane M, Kaysen D, Fahey K, Rapoport J (1994), Looking for childhood-onset schizophrenia: the first 71 cases screened. J Am Acad Child Adolesc Psychiatry 33:636-644
13. Money J, Alexander D (1966), Turner's syndrome: further demonstration of the presence of specific congenital deficiencies. J Med Genet 3:47-48
14. Nielsen J, Wohlert M (1991), Chromosome abnormalities found among 34,910 newborn children: results from a 13 year incidence study in Aarhus, Denmark. Hum Genet 87:81-83
15. Rovet J, Netley C, Bailey J, Keenan M, Stewart D (1995), Intelligence and achievement in children with extra X aneuploidy: a longitudinal perspective. Am J Med Genet 60:356-363
16. Shapiro BA (1997), Whither Down syndrome critical regions? Hum Genet 99:421-423
17. Skuse DH, James RS, Bishop DVM et al. (1997), Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 39:705-708
18. Sperber MA, Salomon L, Collins MH, Stambler M (1972), Childhood schizophrenia and 47,XXY Klinefelter's syndrome. Am J Psychiatry 128:84-92
19. Turner G (1996), Intelligence and the X chromosome Lancet 347:1814-1815
20. Walzer S, Bashir AS, Silbert AR (1991), Cognitive and behavioral factors in the learning disabilities of 47,XYY and 47,XYY boys. In: Birth Defects: Original Article Series. New York: March of Dimes Birth Defects Foundation, pp 45-58
21. Walzer S, Wollf PH, Bowen D et al. (1978), A method for the longitudinal study of behavioral development in infants and children: the early development of XXY children. J Child Psychol Psychiatry 19:213-229
22. Yan W, Jacobsen LK, Krasnewich DM et al. (in press), Chromosome 22 q 11.2 interstitial deletions among childhood-onset schizophrenics and "multidimensionally impaired." Neuropsychiatr Genet