Congenital Anomalies of the Kidney and Urinary tract
Conditions
Interventions
Observation group (congenital kidney and urinary tract malformations group):None
Control group (non-congenital kidney or urinary tract malformation group):None
Sponsors
Peking University First Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Observation group (1) 0 years old< = age<=90 years old, gender is not limited; (2) Imaging diagnosis of congenital kidney and urinary tract malformations (abnormal kidney development: kidney underdevelopment, hypoplasia, dysplasia and ectopic kidney, etc.; Urinary tract obstructive lesions: renal pelvisureteral junction obstruction (UPJO), vesicoureteral reflux (VUR), posterior urethral valve (PUV), etc.; Abnormal collection system: duplicate renal pelvis ureter, giant ureter, ureteral cyst, etc.); (3) Patients or their legal guardians sign written informed consent and agree to provide clinical data and imaging data for this study; (4) Be able to provide complete clinical data and imaging data. 2. Control group (1) 0 years old< = age<=90 years old, gender is not limited; (2) Patients with non-congenital kidney and urinary tract malformations or patients with acquired factors leading to kidney and urinary tract malformations; (3) Patients or their legal guardians sign written informed consent and agree to provide clinical data and imaging data for this study; (4) Be able to provide complete clinical data and imaging data.
Exclusion criteria
Exclusion criteria: 1. Observation group (1) Non-congenital malformations: acquired kidney or urinary tract diseases (such as stones, tumors, post-traumatic malformations) or urinary tract abnormalities secondary to infection, drugs, or metabolic diseases; (2) Lack of necessary imaging data; (3) The image quality is poor and cannot be annotated. (4) Unable to cooperate with follow-up or refuse to provide necessary clinical information 2. Control group (1) Unable to cooperate with follow-up or refuse to provide necessary clinical information; (2) Lack of necessary imaging data; (3) The image quality is poor and cannot be annotated.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Radiological parameters;Subtype classification; | — |
Secondary
| Measure | Time frame |
|---|---|
| Renal function; | — |
Countries
China
Contacts
Public ContactXuesong Li
Peking University First Hospital
Outcome results
None listed