Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies. Issue 2 (25th May 2020)
- Record Type:
- Journal Article
- Title:
- Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies. Issue 2 (25th May 2020)
- Main Title:
- Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies
- Authors:
- Thompson, Talia
Howell, Susan
Davis, Shanlee
Wilson, Rebecca
Janusz, Jennifer
Boada, Richard
Pyle, Laura
Tartaglia, Nicole - Other Names:
- Gravholt Claus H. guestEditor.
Tartaglia Nicole guestEditor.
Disteche Christine guestEditor. - Abstract:
- Abstract: Sex chromosome aneuploidies (SCAs) are the most commonly occurring aneuploidies in children with a collective prevalence rate of 1 in 500 live births. Prior research has documented SCAs are associated with an increased risk for early expressive language and gross motor delays, learning disorders, ADHD, autism spectrum disorder, anxiety, and executive function problems. Although SCAs have been historically underdiagnosed in young children, recent advances in noninvasive prenatal testing have resulted in an increasing nationwide cohort of infants with confirmed diagnoses. Consequently, early childhood support systems must prepare for an influx of children with known risks for associated developmental delays and potential school problems. This national survey aimed to update our understanding of current early childhood intervention services for young children with SCA in the United States and to describe parent perspectives and priorities. Descriptive statistics, chi‐square tests, and logistic regression models controlling for parent education revealed a majority of respondents reported receiving public early childhood intervention services with speech therapy as the most common service. There were significant differences in early childhood intervention services by timing of diagnosis (prenatal vs. postnatal), number of sex chromosomes (trisomy vs. tetra/pentasomy), and geographic location. Parents described interventions as desirable and effective yet also difficultAbstract: Sex chromosome aneuploidies (SCAs) are the most commonly occurring aneuploidies in children with a collective prevalence rate of 1 in 500 live births. Prior research has documented SCAs are associated with an increased risk for early expressive language and gross motor delays, learning disorders, ADHD, autism spectrum disorder, anxiety, and executive function problems. Although SCAs have been historically underdiagnosed in young children, recent advances in noninvasive prenatal testing have resulted in an increasing nationwide cohort of infants with confirmed diagnoses. Consequently, early childhood support systems must prepare for an influx of children with known risks for associated developmental delays and potential school problems. This national survey aimed to update our understanding of current early childhood intervention services for young children with SCA in the United States and to describe parent perspectives and priorities. Descriptive statistics, chi‐square tests, and logistic regression models controlling for parent education revealed a majority of respondents reported receiving public early childhood intervention services with speech therapy as the most common service. There were significant differences in early childhood intervention services by timing of diagnosis (prenatal vs. postnatal), number of sex chromosomes (trisomy vs. tetra/pentasomy), and geographic location. Parents described interventions as desirable and effective yet also difficult to obtain due to issues with the SCA phenotype, lack of provider knowledge, and challenges navigating the intervention systems. Results support the need for enhanced provider training in SCAs, policy change for early childhood intervention qualification criteria for SCA conditions, and collaboration between medical and early childhood settings. … (more)
- Is Part Of:
- American journal of medical genetics. Volume 184:Issue 2(2020)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 184:Issue 2(2020)
- Issue Display:
- Volume 184, Issue 2 (2020)
- Year:
- 2020
- Volume:
- 184
- Issue:
- 2
- Issue Sort Value:
- 2020-0184-0002-0000
- Page Start:
- 414
- Page End:
- 427
- Publication Date:
- 2020-05-25
- Subjects:
- developmental delay -- early childhood intervention -- Klinefelter syndrome -- sex chromosome aneuploidy -- |X and Y variations| early childhood special education
Medical genetics -- Periodicals
616.04205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.c.31785 ↗
- Languages:
- English
- ISSNs:
- 1552-4868
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.940000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13356.xml