Literature DB >> 7473652

Velocardiofacial syndrome: learning difficulties and intervention.

L L Kok1, R T Solman.   

Abstract

Velocardiofacial syndrome, delineated in 1978 by Shprintzen, is a multiple genetic disorder, characterised primarily by cleft palate, cardiovascular anomalies, typical facies, and learning disorders. This syndrome with its recurrent pattern of anomalies has significant implications for education as it is linked to a variety of educationally relevant problems including learning difficulties, behaviour disorders, and speech and language deficits. While clinical research advances and new findings in cytogenetics enable early diagnosis and genetic counselling, ramifications of the syndrome in the field of education are still unknown. Learning difficulties should not be viewed solely as a pathological condition and with data on success of intervention, parents and teachers can be apprised of the information. This paper discusses academic characteristics and the effects of intervention with emphasis on interactive computer based instruction on the development of reading, language, spelling, and numeracy skills. Positive effects of computer based instruction on students' self-esteem, motivation, and competence in computer operational skills were also observed and noted. We are encouraged by the enthusiasms of the students for the system, the development of interest in reading, and the transfer of remedial instruction to classroom performance. Comparison of pretest and post-test results indicated significant improvement in reading ability as measured using Neale Analysis. This improvement is in accordance with results obtained using computer testing of specific subskills in reading/language and mathematics.

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Year:  1995        PMID: 7473652      PMCID: PMC1051635          DOI: 10.1136/jmg.32.8.612

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  8 in total

1.  A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Authors:  D A Driscoll; M L Budarf; B S Emanuel
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

2.  Velo-cardio-facial syndrome: language and psychological profiles.

Authors:  K J Golding-Kushner; G Weller; R J Shprintzen
Journal:  J Craniofac Genet Dev Biol       Date:  1985

3.  Male-to-male transmission of the velo-cardio-facial syndrome: a case report and review of 60 cases.

Authors:  M A Williams; R J Shprintzen; R B Goldberg
Journal:  J Craniofac Genet Dev Biol       Date:  1985

4.  The velo-cardio-facial syndrome: a clinical and genetic analysis.

Authors:  R J Shprintzen; R B Goldberg; D Young; L Wolford
Journal:  Pediatrics       Date:  1981-02       Impact factor: 7.124

5.  Cardiac malformations in the velocardiofacial syndrome.

Authors:  D Young; R J Shprintzen; R B Goldberg
Journal:  Am J Cardiol       Date:  1980-10       Impact factor: 2.778

6.  Computer-based reading and spelling practice for children with learning disabilities.

Authors:  V H van Daal; A van der Leij
Journal:  J Learn Disabil       Date:  1992-03

Review 7.  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

8.  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
  8 in total
  4 in total

1.  Acceptance and commitment therapy in genetic counselling: a case study of recurrent worry.

Authors:  Stephanie Broley
Journal:  J Genet Couns       Date:  2012-12-14       Impact factor: 2.537

Review 2.  22q11 deletion syndrome: a genetic subtype of schizophrenia.

Authors:  A S Bassett; E W Chow
Journal:  Biol Psychiatry       Date:  1999-10-01       Impact factor: 13.382

Review 3.  Phenotype of adults with the 22q11 deletion syndrome: A review.

Authors:  E Cohen; E W Chow; R Weksberg; A S Bassett
Journal:  Am J Med Genet       Date:  1999-10-08

4.  SlgA, encoded by the homolog of the human schizophrenia-associated gene PRODH, acts in clock neurons to regulate Drosophila aggression.

Authors:  Liesbeth Zwarts; Veerle Vulsteke; Edgar Buhl; James J L Hodge; Patrick Callaerts
Journal:  Dis Model Mech       Date:  2017-03-22       Impact factor: 5.758

  4 in total

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