Literature DB >> 12116265

Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalities.

Mary G Linden1, Bruce G Bender.   

Abstract

Children with sex chromosome abnormalities (SCA) are known to be at risk for developmental delays. These risks were identified 2 decades ago by seven international research groups who prospectively followed children ascertained after birth. Subsequently, some of these investigators suggested the course of prenatally identified children with SCA may be different from children in earlier studies. The first such evidence was published by Robinson et al. [1992: Am J Med Genet 44:365-368], who compared 20 prenatally diagnosed children to the original postnatally diagnosed cohort. The following report presents an update and expansion of that research and includes 51 children and adolescents prenatally diagnosed with SCA, now 7-18 years of age. Results confirm that this cohort of prenatally diagnosed children has a milder developmental course than children ascertained postnatally. The study provides new information to health professionals counseling families faced with prenatal diagnosis of SCA. Copyright 2002 Wiley-Liss, Inc.

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Mesh:

Year:  2002        PMID: 12116265     DOI: 10.1002/ajmg.10394

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  26 in total

1.  Social deficits in male children and adolescents with sex chromosome aneuploidy: a comparison of XXY, XYY, and XXYY syndromes.

Authors:  Lisa Cordeiro; Nicole Tartaglia; David Roeltgen; Judith Ross
Journal:  Res Dev Disabil       Date:  2012-03-23

2.  Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosis.

Authors:  Faustina Lalatta; Donatella Quagliarini; Emanuela Folliero; Ugo Cavallari; Barbara Gentilin; Pierangela Castorina; Francesca Forzano; Serena Forzano; Enrico Grosso; Valeria Viassolo; Valeria Giorgia Naretto; Stefania Gattone; Florinda Ceriani; Francesca Faravelli; Luigi Gargantini
Journal:  Eur J Pediatr       Date:  2010-05-15       Impact factor: 3.183

Review 3.  Triple X syndrome: a review of the literature.

Authors:  Maarten Otter; Constance T R M Schrander-Stumpel; Leopold M G Curfs
Journal:  Eur J Hum Genet       Date:  2009-07-01       Impact factor: 4.246

Review 4.  Consensus statement on diagnosis and clinical management of Klinefelter syndrome.

Authors:  A F Radicioni; A Ferlin; G Balercia; D Pasquali; L Vignozzi; M Maggi; C Foresta; A Lenzi
Journal:  J Endocrinol Invest       Date:  2010-12       Impact factor: 4.256

5.  Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.

Authors:  Kristen Wigby; Cheryl D'Epagnier; Susan Howell; Amy Reicks; Rebecca Wilson; Lisa Cordeiro; Nicole Tartaglia
Journal:  Am J Med Genet A       Date:  2016-09-19       Impact factor: 2.802

Review 6.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

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

Review 8.  A review of trisomy X (47,XXX).

Authors:  Nicole R Tartaglia; Susan Howell; Ashley Sutherland; Rebecca Wilson; Lennie Wilson
Journal:  Orphanet J Rare Dis       Date:  2010-05-11       Impact factor: 4.123

9.  "How should I tell my child?" Disclosing the diagnosis of sex chromosome aneuploidies.

Authors:  Anna Dennis; Susan Howell; Lisa Cordeiro; Nicole Tartaglia
Journal:  J Genet Couns       Date:  2014-09-03       Impact factor: 2.537

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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