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Study for children with congenital anomalies of the kidney and urinary tract
Protocol: STUDY00004786
Full Title
Identify gene mutation(s) that may be responsible for congenital anomalies of the kidney and urinary tract
This study enrolls children and young adults with congenital anomalies of the kidney and urinary tract (CAKUT). The purpose of the study is to learn which gene mutation(s) may be responsible for this condition and to eventually find a gene therapy to treat this condition.

We will take samples from your child and also from a family member without this condition. The samples include blood, saliva, cheek swabs, and leftover routine kidney biopsy samples. Study takes place at Oishei Children's Hospital in Buffalo, NY.
Compensation: No
Children and young adults ages 0-21 years old with CAKUT (congenital anomalies of the kidney and urinary tract) seen at Oshei Children's Hospital
Patient's family member without CAKUT.
Age Group: Both Adults and Children
Principal Investigator: xiaoyan wu
Haiping Qiao
+1 716-323-0055
Want to Learn More?

Let us know how the study team can reach you. If you do not hear back within 2 business days, then reach out to the study team directly at the contact information above and someone will assist you.

Your information will be shared only with the research study team and administrative staff for recruitment and will remain confidential. Your information will be stored until study recruitment is closed. Should you no longer want this information to be provided in the aforementioned ways, please contact the study team directly.

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