kidney stone suffer, nephrocalcinosis N20.0
Conditions
Interventions
Group 1: Genetic analysis to investigate relationships between certain mutations and renal stone disease.
Sponsors
Universitätsklinik Leipzig, Department für Innere Medizin, Neurologie und Dermatologie, Klinik für Endokrinologie und Neprhologie
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with renal stone disease, nephrocalcinosis and / or hypercalciuria.
Exclusion criteria
Exclusion criteria: Patients with known causative genetic or non-genetic causative disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Identification of a mutation in a known disease gene and correlation with the clinical phenotype. | — |
Secondary
| Measure | Time frame |
|---|---|
| Identification of so far uncharacterized genes. | — |
Countries
Germany
Contacts
Public ContactDominik Schöb
UKF Freiburg
Outcome results
None listed