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Registry for Patients With WT1 Mutation Associated Diseases


N/A
N/A
N/A
Open (Enrolling)
Both
Denys-Drash Syndrome, Frasier Syndrome, Nephrotic Syndrome, Wilms Tumor

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Trial Information

Registry for Patients With WT1 Mutation Associated Diseases


Inclusion Criteria:



- Germline mutation in WT1 gene

Exclusion Criteria:

- none

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Retrospective

Principal Investigator

Anja Lehnhardt, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Universitätsklinikum Hamburg-Eppendorf

Authority:

Germany: Ethics Commission

Study ID:

WT1 Registry

NCT ID:

NCT01252901

Start Date:

October 2010

Completion Date:

Related Keywords:

  • Denys-Drash Syndrome
  • Frasier Syndrome
  • Nephrotic Syndrome
  • Wilms Tumor
  • WT1
  • Wilms Tumor
  • Denys-Drash Syndrome
  • Nephrotic Syndrome
  • Proteinuria
  • Wilms Tumor
  • Nephrotic Syndrome
  • Denys-Drash Syndrome
  • Frasier Syndrome

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