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Mutation Analysis of 17βhydroxysteroid Dehydrogenase 3 Deficiency

NCT00173654 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2005-12-21

No results posted yet for this study

Summary

To disclose the molecular pathology of our 3 families with 17βHSD3 deficiency.

Conditions

  • Pseudohermaphroditism

Interventions

PROCEDURE

blood drawing

Sponsors & Collaborators

  • National Taiwan University Hospital

    lead OTHER

Principal Investigators

  • Yi-Ching Tung, MD · National Taiwan University Hospital

Eligibility

Min Age
0 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-08-31
Completion
2006-08-31

Countries

  • Taiwan

Study Locations

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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 NCT00173654 on ClinicalTrials.gov