Literature DB >> 8820203

The psychoeducational profile of boys with Klinefelter syndrome.

J Rovet1, C Netley, M Keenan, J Bailey, D Stewart.   

Abstract

Klinefelter syndrome (KS) affects about 1 in 900 males due to an extra X chromosome. Although there are no obvious physical features associated with childhood KS, many boys demonstrate a cognitive deficit in verbal processing. The first section of this article integrates the extant literature on intelligence and achievement outcomes in boys with KS. The second section presents our findings from a 20-year study involving one of the largest unselected cohorts of boys with KS. We followed 36 boys with KS and 33 sibling controls from 6 until 20 years of age. Boys with KS are shown to demonstrate a verbal cognitive deficit and significant underachievement in reading and spelling, as well as in arithmetic. These problems, which are evident from early school years, increase with age such that by late adolescence, boys with KS are four to five grade levels behind. In addition, we also found that they were most likely to have a generalized type of learning disability, with very few boys indicating a pure reading or pure arithmetic problem. They also showed deficits in written language skills and acquisition of knowledge-based subject material were also problematic. Despite significant underachievement and frequent grade failure, many boys with KS had completed high school, and a few were also pursuing postsecondary educations. The discussion section examines how their language-based disability affects comprehension and learning, leading to underachievement.

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Year:  1996        PMID: 8820203     DOI: 10.1177/002221949602900208

Source DB:  PubMed          Journal:  J Learn Disabil        ISSN: 0022-2194


  21 in total

1.  Assessing the risks and benefits of diagnosing genetic conditions with variable phenotypes through population screening: Klinefelter syndrome as an example.

Authors:  Amy Simone Herlihy; Jane Halliday; Rob I McLachlan; Megan Cock; Lynn Gillam
Journal:  J Community Genet       Date:  2010-03-29

2.  Executive function in young males with Klinefelter (XXY) syndrome with and without comorbid attention-deficit/hyperactivity disorder.

Authors:  Nancy Raitano Lee; Gregory L Wallace; Liv S Clasen; Rhoshel K Lenroot; Jonathan D Blumenthal; Samantha L White; Mark J Celano; Jay N Giedd
Journal:  J Int Neuropsychol Soc       Date:  2011-05       Impact factor: 2.892

Review 3.  48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome.

Authors:  Nicole Tartaglia; Natalie Ayari; Susan Howell; Cheryl D'Epagnier; Philip Zeitler
Journal:  Acta Paediatr       Date:  2011-04-08       Impact factor: 2.299

4.  Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies.

Authors:  Talia Thompson; Susan Howell; Shanlee Davis; Rebecca Wilson; Jennifer Janusz; Richard Boada; Laura Pyle; Nicole Tartaglia
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-05-25       Impact factor: 3.908

Review 5.  Recent developments in the application of the nonverbal learning disabilities model.

Authors:  Brenna C McDonald
Journal:  Curr Psychiatry Rep       Date:  2002-10       Impact factor: 5.285

6.  Timing of diagnosis of 47,XXY and 48,XXYY: a survey of parent experiences.

Authors:  Jeannie Visootsak; Natalie Ayari; Susan Howell; Joash Lazarus; Nicole Tartaglia
Journal:  Am J Med Genet A       Date:  2013-01-15       Impact factor: 2.802

7.  Social function in multiple X and Y chromosome disorders: XXY, XYY, XXYY, XXXY.

Authors:  Jeannie Visootsak; John M Graham
Journal:  Dev Disabil Res Rev       Date:  2009

8.  An extra X or Y chromosome: contrasting the cognitive and motor phenotypes in childhood in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.

Authors:  Judith L Ross; Martha P D Zeger; Harvey Kushner; Andrew R Zinn; David P Roeltgen
Journal:  Dev Disabil Res Rev       Date:  2009

Review 9.  The cognitive phenotype in Klinefelter syndrome: a review of the literature including genetic and hormonal factors.

Authors:  Richard Boada; Jennifer Janusz; Christa Hutaff-Lee; Nicole Tartaglia
Journal:  Dev Disabil Res Rev       Date:  2009

Review 10.  Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: a systematic review.

Authors:  Victoria Leggett; Patricia Jacobs; Kate Nation; Gaia Scerif; Dorothy V M Bishop
Journal:  Dev Med Child Neurol       Date:  2010-01-05       Impact factor: 5.449

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