Reaction to Diagnosis and Parental Concerns in Parents of Children and Young Adults With XYY Syndrome

ABSTRACT Background There is a growing interest in exploring parents' views on the benefits of early diagnosis and awareness of sex chromosome trisomies. However, only a few studies focus specifically on the experience of parents of children with XYY syndrome. The present study aimed to assess,...

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Veröffentlicht in:Child : care, health & development health & development, 2024-09, Vol.50 (5), p.e13324-n/a
Hauptverfasser: Zampini, Laura, Zanchi, Paola, Silibello, Gaia, Mastromattei, Domenica, Ajmone, Paola Francesca, Dall'Ara, Francesca, Monti, Federico, Costantino, Maria Antonella, Vizziello, Paola Giovanna
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container_start_page e13324
container_title Child : care, health & development
container_volume 50
creator Zampini, Laura
Zanchi, Paola
Silibello, Gaia
Mastromattei, Domenica
Ajmone, Paola Francesca
Dall'Ara, Francesca
Monti, Federico
Costantino, Maria Antonella
Vizziello, Paola Giovanna
description ABSTRACT Background There is a growing interest in exploring parents' views on the benefits of early diagnosis and awareness of sex chromosome trisomies. However, only a few studies focus specifically on the experience of parents of children with XYY syndrome. The present study aimed to assess, in parents of individuals with XYY, the perceived severity of their children's condition, their level of satisfaction with the disclosure process and their concerns about their children's present and future condition. Methods A national online sample of 56 Italian parents of children and young adults diagnosed with XYY syndrome participated in the study. They filled out a specifically developed online survey that assessed their children's areas of concern, their experience with the disclosure process and their worries about their children's condition. Results Seventy per cent of the parents received a prenatal diagnosis, whereas 30% received a postnatal diagnosis. High individual variability was found in the parent report of their child's condition. The most frequent areas of concern were attention regulation, emotion control and behaviour control. Individuals with a postnatal diagnosis showed more severe profiles. Parents were generally dissatisfied with the disclosure process, with no differences between prenatal and postnatal disclosure. However, more than 50% of the parents who received a prenatal disclosure reported that their child's condition was less severe than they had expected. In contrast, only 11% of the parents with postnatal disclosure reported this situation. Parents' concerns were negatively related to global satisfaction with the disclosure process and the correspondence between current and expected conditions but positively associated with the child's severity level. Conclusions The results suggest that clear and realistic information during the disclosure process to parents is needed in both prenatal and postnatal communication and may alleviate parents' concerns.
doi_str_mv 10.1111/cch.13324
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However, only a few studies focus specifically on the experience of parents of children with XYY syndrome. The present study aimed to assess, in parents of individuals with XYY, the perceived severity of their children's condition, their level of satisfaction with the disclosure process and their concerns about their children's present and future condition. Methods A national online sample of 56 Italian parents of children and young adults diagnosed with XYY syndrome participated in the study. They filled out a specifically developed online survey that assessed their children's areas of concern, their experience with the disclosure process and their worries about their children's condition. Results Seventy per cent of the parents received a prenatal diagnosis, whereas 30% received a postnatal diagnosis. High individual variability was found in the parent report of their child's condition. The most frequent areas of concern were attention regulation, emotion control and behaviour control. Individuals with a postnatal diagnosis showed more severe profiles. Parents were generally dissatisfied with the disclosure process, with no differences between prenatal and postnatal disclosure. However, more than 50% of the parents who received a prenatal disclosure reported that their child's condition was less severe than they had expected. In contrast, only 11% of the parents with postnatal disclosure reported this situation. Parents' concerns were negatively related to global satisfaction with the disclosure process and the correspondence between current and expected conditions but positively associated with the child's severity level. Conclusions The results suggest that clear and realistic information during the disclosure process to parents is needed in both prenatal and postnatal communication and may alleviate parents' concerns.</description><identifier>ISSN: 0305-1862</identifier><identifier>ISSN: 1365-2214</identifier><identifier>EISSN: 1365-2214</identifier><identifier>DOI: 10.1111/cch.13324</identifier><identifier>PMID: 39188018</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adolescent ; Adult ; Attention ; Child ; Child development ; Child, Preschool ; Children ; Children &amp; youth ; Chromosomes ; Concerns ; diagnosis disclosure ; Emotional regulation ; Female ; Genetic disorders ; Health behavior ; Humans ; Italy ; Jacobs syndrome ; Male ; Medical diagnosis ; parental concerns ; Parents ; Parents &amp; parenting ; Parents - psychology ; Postpartum period ; Prenatal care ; Prenatal Diagnosis - psychology ; Severity ; Sex Chromosome Disorders - diagnosis ; Sex Chromosome Disorders - psychology ; sex chromosome trisomies ; Surveys and Questionnaires ; Truth Disclosure ; XXY syndrome ; XYY Karyotype - diagnosis ; XYY Karyotype - psychology ; Young Adult ; Young adults</subject><ispartof>Child : care, health &amp; development, 2024-09, Vol.50 (5), p.e13324-n/a</ispartof><rights>2024 The Author(s). published by John Wiley &amp; Sons Ltd.</rights><rights>2024 The Author(s). 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Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2784-5acae6c4275ae5c3febd145a21afb24ef6157711609f46d68dbe0d455e882ede3</cites><orcidid>0000-0002-0624-4634 ; 0000-0002-2207-0179</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcch.13324$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcch.13324$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,30999,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39188018$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zampini, Laura</creatorcontrib><creatorcontrib>Zanchi, Paola</creatorcontrib><creatorcontrib>Silibello, Gaia</creatorcontrib><creatorcontrib>Mastromattei, Domenica</creatorcontrib><creatorcontrib>Ajmone, Paola Francesca</creatorcontrib><creatorcontrib>Dall'Ara, Francesca</creatorcontrib><creatorcontrib>Monti, Federico</creatorcontrib><creatorcontrib>Costantino, Maria Antonella</creatorcontrib><creatorcontrib>Vizziello, Paola Giovanna</creatorcontrib><title>Reaction to Diagnosis and Parental Concerns in Parents of Children and Young Adults With XYY Syndrome</title><title>Child : care, health &amp; development</title><addtitle>Child Care Health Dev</addtitle><description>ABSTRACT Background There is a growing interest in exploring parents' views on the benefits of early diagnosis and awareness of sex chromosome trisomies. However, only a few studies focus specifically on the experience of parents of children with XYY syndrome. The present study aimed to assess, in parents of individuals with XYY, the perceived severity of their children's condition, their level of satisfaction with the disclosure process and their concerns about their children's present and future condition. Methods A national online sample of 56 Italian parents of children and young adults diagnosed with XYY syndrome participated in the study. They filled out a specifically developed online survey that assessed their children's areas of concern, their experience with the disclosure process and their worries about their children's condition. Results Seventy per cent of the parents received a prenatal diagnosis, whereas 30% received a postnatal diagnosis. High individual variability was found in the parent report of their child's condition. The most frequent areas of concern were attention regulation, emotion control and behaviour control. Individuals with a postnatal diagnosis showed more severe profiles. Parents were generally dissatisfied with the disclosure process, with no differences between prenatal and postnatal disclosure. However, more than 50% of the parents who received a prenatal disclosure reported that their child's condition was less severe than they had expected. In contrast, only 11% of the parents with postnatal disclosure reported this situation. Parents' concerns were negatively related to global satisfaction with the disclosure process and the correspondence between current and expected conditions but positively associated with the child's severity level. 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Zanchi, Paola ; Silibello, Gaia ; Mastromattei, Domenica ; Ajmone, Paola Francesca ; Dall'Ara, Francesca ; Monti, Federico ; Costantino, Maria Antonella ; Vizziello, Paola Giovanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2784-5acae6c4275ae5c3febd145a21afb24ef6157711609f46d68dbe0d455e882ede3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Attention</topic><topic>Child</topic><topic>Child development</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Children &amp; youth</topic><topic>Chromosomes</topic><topic>Concerns</topic><topic>diagnosis disclosure</topic><topic>Emotional regulation</topic><topic>Female</topic><topic>Genetic disorders</topic><topic>Health behavior</topic><topic>Humans</topic><topic>Italy</topic><topic>Jacobs syndrome</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>parental concerns</topic><topic>Parents</topic><topic>Parents &amp; parenting</topic><topic>Parents - psychology</topic><topic>Postpartum period</topic><topic>Prenatal care</topic><topic>Prenatal Diagnosis - psychology</topic><topic>Severity</topic><topic>Sex Chromosome Disorders - diagnosis</topic><topic>Sex Chromosome Disorders - psychology</topic><topic>sex chromosome trisomies</topic><topic>Surveys and Questionnaires</topic><topic>Truth Disclosure</topic><topic>XXY syndrome</topic><topic>XYY Karyotype - diagnosis</topic><topic>XYY Karyotype - psychology</topic><topic>Young Adult</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zampini, Laura</creatorcontrib><creatorcontrib>Zanchi, Paola</creatorcontrib><creatorcontrib>Silibello, Gaia</creatorcontrib><creatorcontrib>Mastromattei, Domenica</creatorcontrib><creatorcontrib>Ajmone, Paola Francesca</creatorcontrib><creatorcontrib>Dall'Ara, Francesca</creatorcontrib><creatorcontrib>Monti, Federico</creatorcontrib><creatorcontrib>Costantino, Maria Antonella</creatorcontrib><creatorcontrib>Vizziello, Paola Giovanna</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library Free Content</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><collection>MEDLINE - Academic</collection><jtitle>Child : care, health &amp; development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zampini, Laura</au><au>Zanchi, Paola</au><au>Silibello, Gaia</au><au>Mastromattei, Domenica</au><au>Ajmone, Paola Francesca</au><au>Dall'Ara, Francesca</au><au>Monti, Federico</au><au>Costantino, Maria Antonella</au><au>Vizziello, Paola Giovanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reaction to Diagnosis and Parental Concerns in Parents of Children and Young Adults With XYY Syndrome</atitle><jtitle>Child : care, health &amp; development</jtitle><addtitle>Child Care Health Dev</addtitle><date>2024-09</date><risdate>2024</risdate><volume>50</volume><issue>5</issue><spage>e13324</spage><epage>n/a</epage><pages>e13324-n/a</pages><issn>0305-1862</issn><issn>1365-2214</issn><eissn>1365-2214</eissn><abstract>ABSTRACT Background There is a growing interest in exploring parents' views on the benefits of early diagnosis and awareness of sex chromosome trisomies. However, only a few studies focus specifically on the experience of parents of children with XYY syndrome. The present study aimed to assess, in parents of individuals with XYY, the perceived severity of their children's condition, their level of satisfaction with the disclosure process and their concerns about their children's present and future condition. Methods A national online sample of 56 Italian parents of children and young adults diagnosed with XYY syndrome participated in the study. They filled out a specifically developed online survey that assessed their children's areas of concern, their experience with the disclosure process and their worries about their children's condition. Results Seventy per cent of the parents received a prenatal diagnosis, whereas 30% received a postnatal diagnosis. High individual variability was found in the parent report of their child's condition. The most frequent areas of concern were attention regulation, emotion control and behaviour control. Individuals with a postnatal diagnosis showed more severe profiles. Parents were generally dissatisfied with the disclosure process, with no differences between prenatal and postnatal disclosure. However, more than 50% of the parents who received a prenatal disclosure reported that their child's condition was less severe than they had expected. In contrast, only 11% of the parents with postnatal disclosure reported this situation. Parents' concerns were negatively related to global satisfaction with the disclosure process and the correspondence between current and expected conditions but positively associated with the child's severity level. Conclusions The results suggest that clear and realistic information during the disclosure process to parents is needed in both prenatal and postnatal communication and may alleviate parents' concerns.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>39188018</pmid><doi>10.1111/cch.13324</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-0624-4634</orcidid><orcidid>https://orcid.org/0000-0002-2207-0179</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Attention
Child
Child development
Child, Preschool
Children
Children & youth
Chromosomes
Concerns
diagnosis disclosure
Emotional regulation
Female
Genetic disorders
Health behavior
Humans
Italy
Jacobs syndrome
Male
Medical diagnosis
parental concerns
Parents
Parents & parenting
Parents - psychology
Postpartum period
Prenatal care
Prenatal Diagnosis - psychology
Severity
Sex Chromosome Disorders - diagnosis
Sex Chromosome Disorders - psychology
sex chromosome trisomies
Surveys and Questionnaires
Truth Disclosure
XXY syndrome
XYY Karyotype - diagnosis
XYY Karyotype - psychology
Young Adult
Young adults
title Reaction to Diagnosis and Parental Concerns in Parents of Children and Young Adults With XYY Syndrome
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