Literature DB >> 32501621

Rare sex chromosome variation 48,XXYY: An integrative review.

Amy A Blumling1, Kristy Martyn1, Amy Talboy1, Sharron Close1.   

Abstract

While the most common Sex Chromosome Aneuploidy (SCA) is 47,XXY, other variations, such as 48,XXYY, are less studied, perhaps due to its rarity. 48,XXYY occurs with an estimated prevalence of 1:18,000-40,000 male births. This SCA is associated with a variety of complex physical, psychological, and neuroanatomical findings. The purpose of this integrative review is to summarize the available evidence related to 48,XXYY and identify gaps in the literature. This study utilized integrative review and PRISMA-guided methodology to search six databases for information pertaining to 48,XXYY. There were no exclusion criteria related to design methodology, given the paucity of available research. Among 397 articles reviewed for potential inclusion, 30 articles remained after inclusion and exclusion criteria were applied. Seven of these articles concentrated solely on participants with 48,XXYY. Literature was summarized into categories of physical phenotype, psychosocial, behavioral, neurocognitive, and brain function. Clinical description of 48,XXYY has evolved over time to develop a deeper understanding of this complex disorder. Large gaps remain, especially a lack of experimental studies, clinical guidelines, and treatments. Additionally, few studies explore methodologies such as interviews or self-report surveys in this population. 48,XXYY presents with a wide spectrum of physical, psychological, and neurocognitive symptoms, and frequently requires complex interdisciplinary care. In order to better understand this disorder and to appropriately treat the individuals affected by it, future research should focus on experimental studies and research that utilizes a variety of methods, including participant interviews and patient-report surveys.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  48,XXYY; integrative review; literature review; sex chromosome aneuploidy

Mesh:

Year:  2020        PMID: 32501621     DOI: 10.1002/ajmg.c.31789

Source DB:  PubMed          Journal:  Am J Med Genet C Semin Med Genet        ISSN: 1552-4868            Impact factor:   3.908


  2 in total

1.  Sex chromosome aneuploidies in 2020-The state of care and research in the world.

Authors:  Claus H Gravholt; Nicole Tartaglia; Christine Disteche
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-06-04       Impact factor: 3.908

2.  A Patient with Moderate Intellectual Disability and 49, XXXYY Karyotype.

Authors:  Willem M A Verhoeven; Jos I M Egger; Sandra Mergler; Ton A A Meijer; Rolph Pfundt; Marjolein H Willemsen
Journal:  Int J Gen Med       Date:  2022-03-10
  2 in total

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