Literature DB >> 16539884

Prevalence of ADHD in children with velocardiofacial syndrome: a preliminary report.

Karen Zagursky1, Ronald A Weller, Naushad Jessani, Jawwad Abbas, Elizabeth B Weller.   

Abstract

Velocardiofacial syndrome (VCFS) is a relatively common multi-anomaly disorder associated with a deletion on chromosome 22. Patients with VCFS have cardiac anomalies, cleft palate, learning problems, and speech and developmental delays. Previous studies found that mood and psychotic illnesses were the most common psychiatric disorders in patients with VCFS. The few studies that have focused solely on children with VCFS, however, have found an increased prevalence of attention-deficit/ hyperactivity disorder (ADHD). This paper reports on a clinical evaluation and a structured interview that were administered to 52 children with VCFS and their parents. The prevalence of ADHD in this sample was approximately 10 times that in the general population. Awareness of the possibility of increased prevalence of ADHD in VCFS, particularly of the inattentive type, is important because it is likely to be overlooked by parents and clinicians. Intervention with these children may halt the progression of psychiatric illness and improve outcome.

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Year:  2006        PMID: 16539884     DOI: 10.1007/s11920-006-0006-2

Source DB:  PubMed          Journal:  Curr Psychiatry Rep        ISSN: 1523-3812            Impact factor:   5.285


  21 in total

1.  Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFS.

Authors:  A Swillen; K Devriendt; E Legius; B Eyskens; M Dumoulin; M Gewillig; J P Fryns
Journal:  J Med Genet       Date:  1997-06       Impact factor: 6.318

2.  Study I: development and criterion validity of the Children's Interview for Psychiatric Syndromes (ChIPS).

Authors:  M Teare; M A Fristad; E B Weller; R A Weller; P Salmon
Journal:  J Child Adolesc Psychopharmacol       Date:  1998       Impact factor: 2.576

3.  Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.

Authors:  Lena Niklasson; Peder Rasmussen; Sólveig Oskarsdóttir; Christopher Gillberg
Journal:  Dev Med Child Neurol       Date:  2002-01       Impact factor: 5.449

Review 4.  Velo-cardio-facial syndrome: a distinctive behavioral phenotype.

Authors:  R J Shprintzen
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2000

5.  Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

Authors:  D F Papolos; G L Faedda; S Veit; R Goldberg; B Morrow; R Kucherlapati; R J Shprintzen
Journal:  Am J Psychiatry       Date:  1996-12       Impact factor: 18.112

6.  Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome.

Authors:  D Gothelf; A Frisch; H Munitz; R Rockah; N Laufer; T Mozes; H Hermesh; A Weizman; M Frydman
Journal:  Schizophr Res       Date:  1999-01-11       Impact factor: 4.939

7.  Variable phenotypes in velocardiofacial syndrome with chromosomal deletion.

Authors:  B Motzkin; R Marion; R Goldberg; R Shprintzen; P Saenger
Journal:  J Pediatr       Date:  1993-09       Impact factor: 4.406

Review 8.  Velo-cardio-facial syndrome: a review of 120 patients.

Authors:  R Goldberg; B Motzkin; R Marion; P J Scambler; R J Shprintzen
Journal:  Am J Med Genet       Date:  1993-02-01

9.  A new syndrome involving cleft palate, cardiac anomalies, typical facies, and learning disabilities: velo-cardio-facial syndrome.

Authors:  R J Shprintzen; R B Goldberg; M L Lewin; E J Sidoti; M D Berkman; R V Argamaso; D Young
Journal:  Cleft Palate J       Date:  1978-01

10.  Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

Authors:  D A Driscoll; N B Spinner; M L Budarf; D M McDonald-McGinn; E H Zackai; R B Goldberg; R J Shprintzen; H M Saal; J Zonana; M C Jones
Journal:  Am J Med Genet       Date:  1992-09-15
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  5 in total

Review 1.  A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment.

Authors:  Opal Ousley; Kimberly Rockers; Mary Lynn Dell; Karlene Coleman; Joseph F Cubells
Journal:  Curr Psychiatry Rep       Date:  2007-04       Impact factor: 5.285

2.  Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.

Authors:  Kelly Schoch; Waverly Harrell; Stephen R Hooper; Edward H Ip; Santiago Saldana; Thomas R Kwapil; Vandana Shashi
Journal:  J Learn Disabil       Date:  2012-05-09

3.  The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder.

Authors:  Arie J Stam; Patricia F Schothorst; Jacob As Vorstman; Wouter G Staal
Journal:  Appl Clin Genet       Date:  2009-03-10

4.  The clinical presentation of attention deficit-hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome.

Authors:  Maria Niarchou; Joanna Martin; Anita Thapar; Michael J Owen; Marianne B M van den Bree
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2015-09-24       Impact factor: 3.568

5.  Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome.

Authors:  A Starnawska; C S Hansen; T Sparsø; W Mazin; L Olsen; M Bertalan; A Buil; J Bybjerg-Grauholm; M Bækvad-Hansen; D M Hougaard; P B Mortensen; C B Pedersen; M Nyegaard; T Werge; S Weinsheimer
Journal:  Transl Psychiatry       Date:  2017-08-29       Impact factor: 6.222

  5 in total

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