Literature DB >> 27832510

The Impact of Living with Klinefelter Syndrome: A Qualitative Exploration of Adolescents and Adults.

Amy Turriff1, Ellen Macnamara2, Howard P Levy3, Barbara Biesecker4.   

Abstract

Klinefelter syndrome (XXY) is a common yet significantly underdiagnosed condition with considerable medical, psychological and social implications. Many health care providers lack familiarity with XXY, resulting in medical management challenges and a limited understanding of the personal impact of the condition. Genetic counselors benefit from understanding the challenges adolescents and men with XXY face to effectively address their medical and psychosocial needs. The purpose of this study was to understand the impact of living with XXY as an adolescent or an adult. Individuals aged 14 to 75 years with self-reported XXY were recruited from online support networks to complete a web-based survey that included open-ended questions. Open-ended responses were coded and analyzed thematically (n = 169 to 210 for each open-ended question). Over half of respondents to the open-ended questions reported challenges in finding health care providers who are knowledgeable about XXY, with many describing an extensive diagnostic odyssey and relief when receiving a diagnosis. Individuals sought support coping with the challenges they face and acknowledgement of the positive aspects of XXY. Recommendations are made for how genetic counseling can enhance quality of life for individuals living with XXY.

Entities:  

Keywords:  47,XXY; Klinefelter syndrome; Psychosocial impact; Sex chromosome aneuploidy

Mesh:

Year:  2016        PMID: 27832510      PMCID: PMC5425317          DOI: 10.1007/s10897-016-0041-z

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  35 in total

1.  Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study.

Authors:  Anders Bojesen; Svend Juul; Claus Højbjerg Gravholt
Journal:  J Clin Endocrinol Metab       Date:  2003-02       Impact factor: 5.958

2.  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

3.  Children and young adults with sex chromosome aneuploidy-- follow-up, clinical and molecular studies. Minaki, Ontario, Canada, June 7-10, 1989.

Authors: 
Journal:  Birth Defects Orig Artic Ser       Date:  1990

4.  Sex chromatin deviations among school children in special classes. A study of prevalence and an investigation of birth histories.

Authors:  B Eriksson
Journal:  J Ment Defic Res       Date:  1972-06

5.  47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling.

Authors:  L Abramsky; J Chapple
Journal:  Prenat Diagn       Date:  1997-04       Impact factor: 3.050

Review 6.  The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome).

Authors:  Nicole Tartaglia; Lisa Cordeiro; Susan Howell; Rebecca Wilson; Jennifer Janusz
Journal:  Pediatr Endocrinol Rev       Date:  2010-12

7.  Phenotype and Adverse Quality of Life in Boys with Klinefelter Syndrome.

Authors:  Sharron Close; Ilene Fennoy; Arlene Smaldone; Nancy Reame
Journal:  J Pediatr       Date:  2015-07-21       Impact factor: 4.406

8.  "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

9.  Psychosocial adaptation of 39 adolescents with sex chromosome abnormalities.

Authors:  B G Bender; R J Harmon; M G Linden; A Robinson
Journal:  Pediatrics       Date:  1995-08       Impact factor: 7.124

10.  The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy.

Authors:  Nicole Tartaglia; Susan Howell; Rebecca Wilson; Jennifer Janusz; Richard Boada; Sydney Martin; Jacqueline B Frazier; Michelle Pfeiffer; Karen Regan; Sarah McSwegin; Philip Zeitler
Journal:  J Multidiscip Healthc       Date:  2015-07-17
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  10 in total

Review 1.  Morbidity in Klinefelter syndrome and the effect of testosterone treatment.

Authors:  Simon Chang; Anne Skakkebaek; Shanlee M Davis; Claus H Gravholt
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-04       Impact factor: 3.908

Review 2.  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

3.  Experiences of individuals receiving a sex chromosome multisomy diagnosis.

Authors:  Jordan P Richardson; Nivedita Ahlawat; Kirsten A Riggan; Sharron Close; Megan A Allyse
Journal:  J Community Genet       Date:  2022-08-19

4.  "There Are Hills and Valleys": Experiences of Parenting a Son With X-Linked Retinoschisis.

Authors:  Amy Turriff; Rosalie Nolen; Celeste D'Amanda; Barbara Biesecker; Catherine Cukras; Paul A Sieving
Journal:  Am J Ophthalmol       Date:  2019-11-23       Impact factor: 5.258

5.  Perspectives of adults with Klinefelter syndrome, unaffected adolescent males, and parents of affected children toward diagnosis disclosure: a Thai experience.

Authors:  Sukrit Suwannachat; Duangrurdee Wattanasirichaigoon; Jiraporn Arunakul; Vilawan Chirdkiatgumchai; Thipwimol Tim-Aroon
Journal:  J Community Genet       Date:  2019-09-04

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.  Navigating Disrupted Puberty: Development and Evaluation of a Mobile-Health Transition Passport for Klinefelter Syndrome.

Authors:  Andrew A Dwyer; Vanessa Héritier; Sofia Llahana; Lauren Edelman; Georgios E Papadakis; Laurent Vaucher; Nelly Pitteloud; Michael Hauschild
Journal:  Front Endocrinol (Lausanne)       Date:  2022-06-24       Impact factor: 6.055

8.  Communicating the diagnosis of Klinefelter syndrome to children and adolescents: when, how, and who?

Authors:  L Aliberti; I Gagliardi; S Bigoni; S Lupo; S Caracciolo; A Ferlini; A M Isidori; M C Zatelli; M R Ambrosio
Journal:  J Community Genet       Date:  2022-03-05

9.  Quality of life in men with Klinefelter syndrome: the impact of genotype, health, socioeconomics, and sexual function.

Authors:  Anne Skakkebæk; Philip J Moore; Simon Chang; Jens Fedder; Claus H Gravholt
Journal:  Genet Med       Date:  2017-07-20       Impact factor: 8.822

10.  'But you don't look sick': a qualitative analysis of the LUPUS UK online forum.

Authors:  Melanie Sloan; Michael Bosley; Moira Blane; Lynn Holloway; Colette Barrere; David D'Cruz; Chanpreet Walia; Felix Naughton; Paul Howard; Stephen Sutton; Caroline Gordon
Journal:  Rheumatol Int       Date:  2020-10-26       Impact factor: 2.631

  10 in total

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