A Study Evaluating the Diagnosis of an X & Y Chromosome Variation


About this study

The purpose of this study is to understand the experiences of parents of children and individuals with an X & Y chromosome variation with the diagnosis and management of their condition, and to determine if the addition of the Clinical Genomics appointment line to the DLMP report assists patients in their next steps of care.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Parent of a child diagnosed with an X & Y chromosome variation.
  • Individual of age 18+ diagnosed with an X & Y chromosome variation.
  • Previous appointment with Clinical Genomics at Mayo Clinic.

Exclusion Criteria: 

  • No diagnosis of relevant condition.
  • Individuals younger than 18 years old.
  • Has not seen a provider in Clinical Genomics at Mayo Clinic.


Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Megan Allyse, Ph.D.

Contact us for the latest status

Contact information:

Kirsten Riggan M.S., M.A.



More information


Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available


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