EXtraordinarY Kids

EXtraordinarY Kids The eXtraordinarY Kids Group serves to connect families to ongoing clinic and research opportunities!

We are training the next generation! Maddy Halseth was accepted to present her research in genetic counseling at the Ame...
04/29/2026

We are training the next generation! Maddy Halseth was accepted to present her research in genetic counseling at the American College of Medical Genetics Meeting in Baltimore, MD. Maddy interviewed parents participating in the eXtraordinarY Babies Study to better understand how parents perceived various social supports when navigating a prenatal diagnosis. Way to go Maddy! EXtraordinarY Kids, Living with XXY AXYSGenetic.org, My XXY, Chromodiversity Foundation

Hot off the Press!Clinical research in X&Y Variations (also called SCAs) has expanded over the past two decades, but it ...
04/12/2026

Hot off the Press!
Clinical research in X&Y Variations (also called SCAs) has expanded over the past two decades, but it is unclear whether the populations included in these studies reflect the demographic diversity of those affected. We conducted a systematic review of global clinical research on SCAs published in English between January 2004 and May 2024. This systematic review reveals persistent gaps in the demographic reporting and representation of participants in SCA research. To ensure that research findings are equitable and clinically relevant, future studies should adopt standardized demographic reporting and prioritize inclusive enrollment strategies to reflect the full spectrum of individuals with SCAs. See comments for more details.

Hot off the press! This publication highlights data about neurodevelopment disorders (NDD) and mental health conditions ...
04/10/2026

Hot off the press! This publication highlights data about neurodevelopment disorders (NDD) and mental health conditions (MH) comparing 2145 girls with Turner syndrome to age-matched controls at 6 U.S. pediatric health systems. Results show that girls with TS had significantly higher odds of an NDD diagnosis, particularly for speech-­ language, motor, learning, and attentional disorders. Increased odds were also observed for autism spectrum disorder (ASD) and intellectual developmental disorder (IDD), though these remained relatively uncommon. In contrast, MH diagnoses, such as anxiety and mood disorders, were not more prevalent in TS compared to controls. These results support the need for proactive neurodevelopmental screening for girls with TS. Additional research is needed to understand whether MH symptoms are underdiagnosed, present differently, or emerge later in development in youth with TS. See comments for more details.

02/20/2026

Less than one month left to apply!! The NASCARR Career Enhancement Postdoctoral Fellowship offers a 12-month, mentored research experience focused on s*x chromosome aneuploidies (SCA) at one or more NASCARR sites. Fellows engage in hands-on research, attend the national RDCRN Annual Meeting and NASCARR Annual Symposium, and gain access to NASCARR and RDCRN Early Career resources. Applicants must develop a research and training plan with a NASCARR Senior Faculty mentor that aligns with the program’s goal of cultivating independent SCA researchers and commit at least 50% effort to fellowship-related research and career development. The program welcomes candidates from all disciplines relevant to SCA care—including translational research, medical and surgical specialties, dentistry, psychology, and allied health professions—and prioritizes projects that advance clinical trial readiness. Eligible applicants must hold an MD, DDS, DO, PhD, PsyD, DPT, or equivalent terminal degree. Applications are due March 15, 2026. Apply today: https://grants.rarediseasesnetwork.org/grants/NASCARRpostdoc

The Network for Advancing S*x Chromosome Aneuploidy Research Readiness (NASCARR) is a consortium of academic centers acr...
02/14/2026

The Network for Advancing S*x Chromosome Aneuploidy Research Readiness (NASCARR) is a consortium of academic centers across the U.S. who share the goals of improving the lives of individuals with s*x chromosome aneuploidies by advancing innovative research, clinical expertise and education through collaborations between scientists, health care providers, and patient advocacy organizations.

How NASCARR Can Help Individuals and Families:
+Learn more about s*x chromosome aneuploidy conditions
+Quickly connect with experts in your area who can help
+Learn about treatment options and new research studies
+Answer questions your physician may have about s*x chromosome aneuploidies
+Connect with patient advocacy (support) groups for s*x chromosome aneuploidies

See Comments to learn more!

02/13/2026

New funding opportunity for professionals who are interested in research in s*x chromosome aneuploidies (SCAs)! The Network for Advancing S*x Chromosome Aneuploidy Research Readiness (NASCARR) Career Enhancement Post-Doctoral Fellowship supports a 12-month, mentored research experience focused on SCAs at one or more NASCARR sites. See Comments to learn more!




02/13/2026

New funding opportunity for post-docs to do research in s*x chromosome aneuploidies (SCAs)! The Network for Advancing S*x Chromosome Aneuploidy Research Readiness (NASCARR) Career Enhancement Post-Doctoral Fellowship supports a 12-month, mentored research experience focused on SCAs at one or more NASCARR sites. See comments to learn more!




02/11/2026

Applications for the Network for Advancing S*x Chromosome Aneuploidy Research Readiness (NASCARR) Summer Research Internship are open! See Comments for how to learn more.

Hot off the press! This publication highlights clinical data from 1279 children with XXY helped establish the first ever...
01/07/2026

Hot off the press! This publication highlights clinical data from 1279 children with XXY helped establish the first ever growth charts specific to XXY illustrating the unique growth trajectories of this population. Our findings align with previously well established features of tall stature and obesity, but also demonstrate greater variability in growth than previously appreciated. These reference curves offer clinicians a valuable tool to provide individualized care and anticipatory guidance, determine if further evaluation may be warranted, and assess impact of clinical interventions on growth outcomes.

We are actively recruiting women who have had a positive screening result for an X&Y chromosome variation. Please reach ...
12/11/2025

We are actively recruiting women who have had a positive screening result for an X&Y chromosome variation. Please reach out to learn more by contacting [email protected]


CU Anschutz researchers are seeking volunteers who are currently pregnant with a fetus diagnosed with a s*x chromosome a...
11/13/2025

CU Anschutz researchers are seeking volunteers who are currently pregnant with a fetus diagnosed with a s*x chromosome aneuploidy, such as Turner syndrome (45,X) or Klinefelter Syndrome (47,XXY) to participate in a study using umbilical cord tissue, which is normally discarded after delivery. Participation is voluntary and involves coordinated sample collection at delivery. Contact [email protected] for more information.


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Denver, CO

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Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

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+17207776630

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