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Genetic Findings in a Chinese Family With Axenfeld-Rieger Syndrom

NCT03009188 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 9

Last updated 2017-01-04

No results posted yet for this study

Summary

Axenfeld-Rieger syndrome (ARS) is a rare autosomal dominant disorder, characterized by anterior segment abnormalities and systemic abnormalities. To date,two major genes, forkhead box C1 (FOXC1) on chromosome 6p25 and pituitary homeobox 2 (PITX2) on chromosome 4q25, have been demonstrated to cause ARS. In this study, we performed complete ophthalmologic examinations and analysis of FOXC1 and PITX2 of a Chinese family with ARS.

Conditions

  • Genetic Findings in a Chinese Family With ARS

Sponsors & Collaborators

  • Aier Eye Hospital, Changsha

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-07-31
Primary Completion
2016-12-31
Completion
2016-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03009188 on ClinicalTrials.gov