Q62.12
Congenital occlusion of ureterovesical orifice
Clinical Classification Guidelines
Medical Intelligence & Overview
Congenital occlusion of the ureterovesical orifice is a rare birth defect affecting the connection between the ureter and the bladder. This condition involves a blockage at the point where the ureter—the tube carrying urine from the kidney to the bladder—enters the bladder. The occlusion can disrupt normal urine flow, potentially leading to complications such as urinary tract infections, kidney damage, or hydronephrosis. Recognizing this condition early is essential for effective management and treatment.
Causes & Symptoms
Clinical Causes: Developmental abnormalities during fetal growth alter the formation of the ureter-bladder junction. Genetic factors may contribute to improper formation of the urinary tract. Environmental influences during pregnancy that interfere with normal urinary system development.
Key Symptoms: Difficulty urinating or urinary retention Recurrent urinary tract infections (UTIs) Flank pain or discomfort in the side or back Swelling or enlargement of the affected kidney (hydronephrosis) Poor urine stream in infants or children In some cases, no noticeable symptoms until complications emerge
Diagnostic & Treatment
Diagnosis Path: Diagnosis typically involves a combination of medical history review, physical examination, and diagnostic imaging. These may include:
Treatment Protocols: Treatment options aim to restore normal urine flow and prevent kidney damage. Approaches can include:
Clinical Advice & FAQs
Billing Guidance
Is Q62.12 a billable ICD-10 code?
Yes, Q62.12 is a specific, billable code that can be used to indicate a diagnosis for reimbursement purposes.
Documentation
How do I report Q62.12?
Clinical documentation must specify the nature of Congenital occlusion of ureterovesical orifice and any associated comorbidities for accurate reporting.
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