Literature DB >> 6723104

The development of four unselected 47,XYY boys.

B G Bender, M H Puck, J A Salbenblatt, A Robinson.   

Abstract

Four infants identified through neonatal screening programs are an unselected sample of 47,XYY boys. No consistent physical stigmata or medical disorders were identified. Three have increased height. All four demonstrated problems in motor and language development. Although their intelligence is within the average range, all four have language-related learning disorders requiring special education. Mild depression was apparent in all four, perhaps as a secondary result of their learning disorders. Some of the problems seen in the propositi are found in milder forms in other family members, leading to the hypothesis that their karyotype may heighten vulnerability to pre-existing familial conditions. Similarities between these findings and results from seven other study centers with a total of 42 47,XYY boys are noted. Parents of a prenatally diagnosed 47,XYY fetus seen in our center are informed that the extra Y chromosome represents a risk factor for these problems, but that environment remains a primary force in shaping their child's development.

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Year:  1984        PMID: 6723104     DOI: 10.1111/j.1399-0004.1984.tb02013.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  9 in total

1.  Y chromosome gene copy number and lack of autism phenotype in a male with an isodicentric Y chromosome and absent NLGN4Y expression.

Authors:  Judith L Ross; Luke Bloy; Timothy P L Roberts; Judith Miller; Chao Xing; Lawrence A Silverman; Andrew R Zinn
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2019-06-03       Impact factor: 3.568

2.  Abnormal Auditory Mismatch Fields in Children and Adolescents with 47,XYY Syndrome.

Authors:  Junko Matsuzaki; Luke Bloy; Lisa Blaskey; Judith Miller; Emily S Kuschner; Matthew Ku; Marissa Dipiero; Megan Airey; J Christopher Edgar; David Embick; Judith L Ross; Timothy P L Roberts
Journal:  Dev Neurosci       Date:  2019-07-05       Impact factor: 2.984

3.  Oral health management of a patient with 47,XYY syndrome.

Authors:  Altaf Hussain Shah; B S Manjunatha; Naif A Bindayel; Rita Khounganian
Journal:  BMJ Case Rep       Date:  2013-12-05

4.  Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features.

Authors:  J L Ross; N Tartaglia; D E Merry; M Dalva; A R Zinn
Journal:  Genes Brain Behav       Date:  2015-02-01       Impact factor: 3.449

5.  Behavioral and social phenotypes in boys with 47,XYY syndrome or 47,XXY Klinefelter syndrome.

Authors:  Judith L Ross; David P Roeltgen; Harvey Kushner; Andrew R Zinn; Allan Reiss; Martha Zeger Bardsley; Elizabeth McCauley; Nicole Tartaglia
Journal:  Pediatrics       Date:  2012-03-12       Impact factor: 7.124

6.  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 7.  Effects of sex chromosome aneuploidies on brain development: evidence from neuroimaging studies.

Authors:  Rhoshel K Lenroot; Nancy Raitano Lee; Jay N Giedd
Journal:  Dev Disabil Res Rev       Date:  2009

8.  47,XYY syndrome: clinical phenotype and timing of ascertainment.

Authors:  Martha Zeger Bardsley; Karen Kowal; Carly Levy; Ania Gosek; Natalie Ayari; Nicole Tartaglia; Najiba Lahlou; Breanna Winder; Shannon Grimes; Judith L Ross
Journal:  J Pediatr       Date:  2013-06-27       Impact factor: 4.406

9.  Criminality in men with Klinefelter's syndrome and XYY syndrome: a cohort study.

Authors:  Kirstine Stochholm; Anders Bojesen; Anne Skakkebæk Jensen; Svend Juul; Claus Højbjerg Gravholt
Journal:  BMJ Open       Date:  2012-02-22       Impact factor: 2.692

  9 in total

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