This study is being done to obtain pathology reports from all patients in the Dent disease registry who have had a kidney biopsy. The investigator will collect the biopsy slides and reports in an attempt to determine if they have any common findings.
If the patient agrees to be in the study, the patient will be asked to participate in the following: * Sign a consent form indicating the patient's willingness to participate. * Provide a signed medical release form allowing the investigator to request your official kidney biopsy reports, and also allowing the investigator to request the original slides for review. At the end of the study, all slides will be returned to the referring facility. * The investigator will also review your medical record
Study Type
OBSERVATIONAL
Enrollment
20
Mayo Clinic
Rochester, Minnesota, United States
Biopsy changes
The primary outcome will be to determine the number of glomeruli, percent globally sclerotic glomeruli, percent focally sclerotic glomeruli, and the severity of interstitial fibrosis (none, mild, moderate, severe) and interstitial crystals (none, mild, moderate, severe)
Time frame: 2 years
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