Literature DB >> 21226761

Postnatal screening for Klinefelter syndrome: is there a rationale?

Amy S Herlihy1, Lynn Gillam, Jane L Halliday, Robert I McLachlan.   

Abstract

UNLABELLED: Diagnosis of Klinefelter syndrome (KS) allows for timely beneficial interventions across the lifespan. Most cases currently remain undiagnosed because of low awareness of KS amongst health professionals, the hesitancy of men to seek medical attention and its variable clinical presentation. Given these barriers, population-based genetic screening provides an approach to comprehensive and early detection. We examine current evidence regarding risks and benefits of diagnosing KS at different ages.
CONCLUSION: There is a lack of evidence regarding the influence of age at diagnosis on adult outcomes that can only be obtained through a pilot screening programme.
© 2011 The Author(s)/Acta Paediatrica © 2011 Foundation Acta Paediatrica.

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Year:  2011        PMID: 21226761     DOI: 10.1111/j.1651-2227.2011.02151.x

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  8 in total

1.  A qualitative exploration of mothers' and fathers' experiences of having a child with Klinefelter syndrome and the process of reaching this diagnosis.

Authors:  Elyssia Bourke; Pamela Snow; Amy Herlihy; David Amor; Sylvia Metcalfe
Journal:  Eur J Hum Genet       Date:  2013-05-22       Impact factor: 4.246

2.  Preserving children's fertility: two tales about children's right to an open future and the margins of parental obligations.

Authors:  Daniela Cutas; Kristien Hens
Journal:  Med Health Care Philos       Date:  2015-05

Review 3.  Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention.

Authors:  Nicole Tartaglia; Susan Howell; Shanlee Davis; Karen Kowal; Tanea Tanda; Mariah Brown; Cristina Boada; Amanda Alston; Leah Crawford; Talia Thompson; Sophie van Rijn; Rebecca Wilson; Jennifer Janusz; Judith Ross
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-07       Impact factor: 3.908

4.  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

5.  Novel methylation specific real-time PCR test for the diagnosis of Klinefelter syndrome.

Authors:  Akanksha Mehta; Anna Mielnik; Peter N Schlegel; Darius A Paduch
Journal:  Asian J Androl       Date:  2014 Sep-Oct       Impact factor: 3.285

6.  The Lived Experience of Klinefelter Syndrome: A Narrative Review of the Literature.

Authors:  Esmée Sinéad Hanna; Tim Cheetham; Kristine Fearon; Cathy Herbrand; Nicky Hudson; Kevin McEleny; Richard Quinton; Eleanor Stevenson; Scott Wilkes
Journal:  Front Endocrinol (Lausanne)       Date:  2019-11-26       Impact factor: 5.555

7.  Rapid screening for Klinefelter syndrome with a simple high-resolution melting assay: a multicenter study.

Authors:  Dong-Mei Fu; Yu-Lin Zhou; Jing Zhao; Ping Hu; Zheng-Feng Xu; Shi-Ming Lv; Jun-Jie Hu; Zhong-Min Xia; Qi-Wei Guo
Journal:  Asian J Androl       Date:  2018 Jul-Aug       Impact factor: 3.285

8.  Changes in the cohort composition of turner syndrome and severe non-diagnosis of Klinefelter, 47,XXX and 47,XYY syndrome: a nationwide cohort study.

Authors:  Agnethe Berglund; Mette Hansen Viuff; Anne Skakkebæk; Simon Chang; Kirstine Stochholm; Claus Højbjerg Gravholt
Journal:  Orphanet J Rare Dis       Date:  2019-01-14       Impact factor: 4.123

  8 in total

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