Literature DB >> 32449585

Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies.

Talia Thompson1,2, Susan Howell1,2, Shanlee Davis1,2, Rebecca Wilson1,2, Jennifer Janusz1,2, Richard Boada1,2, Laura Pyle1,3, Nicole Tartaglia1,2.   

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 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.
© 2020 Wiley Periodicals, Inc.

Entities:  

Keywords:  Klinefelter syndrome; developmental delay; early childhood intervention; sex chromosome aneuploidy; |X and Y variations| early childhood special education

Mesh:

Year:  2020        PMID: 32449585      PMCID: PMC7413639          DOI: 10.1002/ajmg.c.31785

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


  43 in total

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Journal:  J Dev Behav Pediatr       Date:  2017-04       Impact factor: 2.225

3.  Population-based trends in the prenatal diagnosis of sex chromosome aneuploidy before and after non-invasive prenatal testing.

Authors:  Allanah Howard-Bath; Alice Poulton; Jane Halliday; Lisa Hui
Journal:  Prenat Diagn       Date:  2018-10-30       Impact factor: 3.050

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Journal:  Prenat Diagn       Date:  1997-04       Impact factor: 3.050

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8.  Mother-Infant Interaction and Child Brain Morphology: A Multidimensional Approach to Maternal Sensitivity.

Authors:  Annie Bernier; Fanny Dégeilh; Élizabel Leblanc; Véronique Daneault; Heidi N Bailey; Miriam H Beauchamp
Journal:  Infancy       Date:  2018-10-14

9.  Practice Bulletin No. 163: Screening for Fetal Aneuploidy.

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Journal:  Obstet Gynecol       Date:  2016-05       Impact factor: 7.661

10.  Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

Authors:  Bradford Coffee; Krayton Keith; Igor Albizua; Tamika Malone; Julie Mowrey; Stephanie L Sherman; Stephen T Warren
Journal:  Am J Hum Genet       Date:  2009-10       Impact factor: 11.025

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  4 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

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.  Supporting students with sex chromosome aneuploidies in educational settings: Results of a nationwide survey.

Authors:  Talia Thompson; Shanlee Davis; Jennifer Janusz; Erin Frith; Laura Pyle; Susan Howell; Richard Boada; Rebecca Wilson; Nicole Tartaglia
Journal:  J Sch Psychol       Date:  2022-06-28

4.  'I Wish the School Had a Better Understanding of the Diagnosis': parent perspectives on educational needs of students with sex chromosome aneuploidies.

Authors:  Talia Thompson; Nicole Stinnett; Nicole Tartaglia; Shanlee Davis; Jennifer Janusz
Journal:  J Res Spec Educ Needs       Date:  2022-03-13
  4 in total

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