GENETICS

See also: Tumors

 

The maximum percentage of comorbidity

Miscellaneous

  1. McConville BJ, Length of the Y chromosome and chromosomal variants in inpatient children with psychiatric disorders, Can J Psychiatry. 1983
  2. Weinberg WA, Primary disorder of vigilance, J Pediatr. 1990
  3. Hochreutener H, Dubowitz syndrome, Monatsschr Kinderheilkd. 1990
  4. Pueschel SM, Behavioural observations in children with Down's syndrome, J Ment Defic Res. 1991 [50%]
  5. Mayes SD, The relationship of HIV status, type of coagulation disorder, and school absenteeism to cognition, educational performance, mood, and behavior of boys with hemophilia, J Genet Psychol. 1996 [28,3%]
  6. Shaffer LG, A clinical and molecular study of mosaicism for trisomy 17, Hum Genet. 1996
  7. Steyaert J, A study of the cognitive and psychological profile in 16 children with congenital or juvenile myotonic dystrophy, Clin Genet. 1997
  8. Page T, Developmental disorder associated with increased cellular nucleotidase activity, Proc Natl Acad Sci U S A. 1997
  9. Niedermeyer E., Frontal lobe disinhibition, Rett syndrome and attention deficit hyperactivity disorder, Clin Electroencephalogr. 2001
  10. Berry GT, Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiency, J Inherit Metab Dis. 2001
  11. Zelnik N, Range of neurologic disorders in patients with celiac disease, Pediatrics. 2004
  12. Le Caignec C, Inherited ring chromosome 8 without loss of subtelomeric sequences, Ann Genet. 2004
  13. Orrico Alfredo, Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q), American Journal of Medical Genetics, 2005
  14. Lin JJ, Psychological presentations without hepatic involvement in Wilson disease, Pediatr Neurol. 2006
  15. D'Onofrio BM et al, Paternal Age at Childbearing and Offspring Psychiatric and Academic Morbidity, JAMA Psychiatry 2014


  16. Phenylketonuria

  17. Diamond A, Phenylalanine levels of 6-10 mg/dl may not be as benign as once thought, Acta Paediatr Suppl. 1994
  18. Weglage J, Deficits in selective and sustained attention processes in early treated children with phenylketonuria..., Eur J Pediatr. 1996
  19. Diamond A, Prefrontal cortex cognitive deficits in children treated early and continuously for PKU, Monogr Soc Res Child Dev. 1997
  20. Huijbregts S, Inhibition of prepotent responding and attentional flexibility in treated phenylketonuria, Dev Neuropsychol. 2002
  21. Huijbregts SC, Sustained attention and inhibition of cognitive interference in treated phenylketonuria: associations with concurrent and lifetime phenylalanine concentrations, Neuropsychologia. 2002
  22. Antshel KM, Timing is everything: executive functions in children exposed to elevated levels of phenylalanine, Neuropsychology 2003

  23. Velocardiofacial syndrome

  24. Papolos DF, Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome..., Am J Psychiatry. 1996
  25. Carlson C, Molecular analysis of velo-cardio-facial syndrome patients with psychiatric disorders, Am J Hum Genet. 1997
  26. Sugama S, Morphometry of the head of the caudate nucleus in patients with velocardiofacial syndrome (del 22q11.2), Acta Paediatr. 2000
  27. Niklasson L, Neuropsychiatric disorders in the 22q11 deletion syndrome, Genet Med. 2001
  28. Niklasson L, Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects, Dev Med Child Neurol. 2002
  29. Antshel KM, Behavior and corpus callosum morphology relationships in velocardiofacial syndrome, Psychiatry Res. 2005
  30. Zagursky K, Prevalence of ADHD in Children with Velocardiofacial Syndrome: A Preliminary Report, Curr Psychiatry Rep. 2006


  31. Prade-Willi syndrome

  32. Gross-Tsur V, Prader-Willi syndrome: medical, emotional and cognitive facets, Harefuah. 2000
  33. Gross-Tsur V, Cognition, attention, and behavior in Prader-Willi syndrome, J Child Neurol. 2001
  34. Thomas JA, Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13..., Am J Med Genet A. 2003
  35. Wigren M, ADHD symptoms and insistence on sameness in Prader-Willi syndrome, J Intellect Disabil Res. 2005


  36. Williams-Beuren syndrome

  37. NINDS Williams Syndrome Information Page
  38. Pascual-Castroviejo I et al, Williams-Beuren syndrome: presentation of 82 cases, An Pediatr (Barc). 2004
  39. Leyfer OT et al, Prevalence of psychiatric disorders in 4 to 16-year-olds with Williams syndrome, Am J Med Genet B Neuropsychiatr Genet. 2006
  40. Rhodes SM et al, Attention-deficit/hyperactivity disorder and Williams syndrome, J Clin Exp Neuropsychol. 2011

 

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