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Genetic testing for von Hippel-Lindau disease

Genetic testing for von Hippel-Lindau disease - Genetic testing for von Hippel-Lindau disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000002694
Enrollment
100
Registered
2009-11-01
Start date
2009-09-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

von Hippel-Lindau (VHL) disease

Interventions

None listed

Sponsors

Yokohama City University Graduate School of Medicine
Lead Sponsor
Department of Neurosurgery, Yokohama City University School of Medicine
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. patients clinically diagnosed as VHL disease 2. presymptomatic members of VHL families 3. patients suspected VHL disease

Exclusion criteria

Exclusion criteria: none

Design outcomes

Primary

MeasureTime frame
germline mutation detection for von Hippel-Lindau disease (VHL) gene

Secondary

MeasureTime frame
optimal patient follow-up based on the phenotype/genotype correlation study

Countries

Japan

Contacts

Public ContactMasahiro YAO

Yokohama City University Graduate School of Medicine Urology and Molecular Genetics

masayao@med.yokohama-cu.ac.jp045-787-2679

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026