Autistic symptoms among children and young adults with isodicentric chromosome 15

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 81, Issue 5, 1998, Pages 428-433

  Rineer, Suzanne ^a   Finucane, Brenda ^a   Simon, Elliott W ^a  

^a Elwyn   (United States)

Author keywords

Autism; Inverted duplication 15; Isodicentric 15 syndrome; Mental retardation

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; CHILD; CHROMOSOME 15; CLINICAL ARTICLE; FEMALE; GENE DUPLICATION; GENE LOCATION; GENETIC LINKAGE; HUMAN; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL;

ADULT; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 15; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE;

EID: 0031660251     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980907)81:5<428::AID-AJMG12>3.0.CO;2-E     Document Type: Article

References (25)

1. American Psychiatric Association (1987): "Diagnostic and Statistical Manual of Mental Disorders, 3rd Edition-Revised." Washington, DC: American Psychiatric Association: 38-39.
2. American Psychiatric Association (1994): "Diagnostic and Statistical Manual of Mental Disorders, 4th Edition." Washington, DC: American Psychiatric Association: 66-71.
3. Autism Society of America (1994): Definition of Autism. The advocate: Newsletter of the Autism Society of America, 26(2), 3. Silver Spring, MD: Author.
4. Baker P, Piven J, Schwartz S, Patil S (1994): Brief report: Duplication of chromosome 15q11-13 in two individuals with autistic disorder. J Autism Dev Disord 24:529-535.
5. Buckton KE, Spowart G, Newton MS, Evans HJ (1985): Forty-four probands with an additional "marker" chromosome. Hum Genet 69:353-370.
6. Bundey S, Hardy C, Vickers S, Kilpatrick MW, Corbett JA (1994): Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia. Dev Med Child Neurol 36:736-742.
7. Cheng S, Spinner NB, Zackai EH, Knoll JHM (1994): Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients. Am J Hum Genet 55:753-759.
8. Cook EH, Lindgren V, Leventhal L, Courchesne R, Lincoln A, Shulman C, Lord C, Courchesne E (1997): Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet 60:928-934.
9. Fletjer WL, Bennett-Baker PE, Ghaziuddin M, McDonald M, Sheldon S, Gorski JL (1996): Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation. Am J Med Genet 61:182-187.
10. Ghaziuddin M, Sheldon S, Venkataraman S, Tsai L, Ghaziuddin N (1993): Autism associated with tetrasomy 15: A further report. Eur J Child Adolesc Psychiatry 2:226-230.
11. Gillberg C, Steffenburg S, Wahlström J, Gillberg IC, Sjöstedt A, Martinsson T, Liedgren S, Eeg-Olofsson O (1991): Autism associated with marker chromosome. J Am Acad Child Adolesc Psychiatry 30:489-494.
12. Gilliam J (1995): "The Gilliam Autism Rating Scale." Austin, TX: Pro-Ed 1-31.
13. Grammatico P, DiRosa C, Roccella M, Falcolini M, Pelliccia A, Roccella F, Del Porto G (1994): Inv dup(15): Contribution to the clinical definition of phenotype. Clin Genet 46:233-237.
14. Krug DA, Arick JR, Almond PJ (1993): "Autism Screening Instrument for Educational Planning," 2nd ed. Austin, TX: Pro-Ed.
15. Pericak-Vance MA, Wolpert CM, Menold MM, Bass MP, Delong GR, Bcaty LM, Zimmerman A, Potter N, Gilbert JR, Vance JM, Wright HH, Abramson RK, Cuccaro ML (1997): Linkage evidence supports the involvement of chromosome 15 in autistic disorder. Am J Hum Genet 61:40.
16. Robinson WP, Binkert F, Gine R, Vazquez C, Müller W, Rosenkranz W, Schinzel A (1993a): Clinical and molecular analysis of five inv dup(15) patients. Eur J Hum Genet 1:37-50.
17. Robinson WP, Wagstaff J, Bernasconi F, Baccichetti C, Artifoni L, Franzoni E, Suslak L, Shih LY, Aviv H, Schinzel AA (1993b): Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome. J Med Genet 30:756-760.
18. Schinzel A (1981): Particular behavioral symptomatology in patients with rarer autosomal chromosome aberrations. In Schmid W, Nielsen, J (eds): "Human Behavior and Genetics." Amsterdam: Elsevier/North Holland. 195-210.
19. Schinzel A (1990): Autistic disorder and additional inv dup(15)(pter→q13) chromosome. Am J Med Genet 35:447.
20. Schreck RR, Breg WR, Erlanger BP, Miller OJ (1977): Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15. Hum Genet 36:1-12.
21. Schroer RJ, Phelan MC, Michaelis RC, Crawford EC, Skinner SA, Cuccaro M, Simensen RJ, Bishop J, Skinner C, Fender D, Stevenson RE (1998): Autism and maternally derived aberrations of chromosome 15q. Am J Med Genet 76:327-336.
22. Smith A, Einfeld S (1986): Isochromosome 15 with behaviour disorder. Hum Genet 72:188.
23. Steffenburg S, Gillberg C (1989): A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry 30:405-416.
24. Wahlström J, Steffenburg S, Hellgren L, Gillberg C (1989): Chromosome findings in twins with infantile autism. Am J Med Genet 11:400-402.
25. Wisniewski L, Hassold T, Heffelfinger J, Higgins JV (1979): Cytogenetic and clinical studies in five cases of inv dup(15). Hum Genet 50:259-270.