Congenital Hydronephrosis in the Newborn is a commonly detected renal abnormality found on in utero imaging in up to 5% of pregnancies. The most common etiology for isolated hydronephrosis, i.e. not associated with other urinary tract abnormalities, is transient or physiologic (50-70%) and likely to resolve within the first 2 years of life. The degree of dilation, however, may indicate the presence of genitourinary pathology such as ureteropelvic junction obstruction, vesicoureteral reflux, ureterocele, ectopic ureter, or posterior urethral valve.
 

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These guidelines are intended solely for the use of healthcare professionals who are licensed to practice medicine. This material is not intended to replace professional medical judgment, prescribing information or consultation with a medical professional. Any health care provider using this material acknowledges full responsibility for the medical care and treatment of patients. All health care providers are solely responsible for confirming the accuracy, timeliness, completeness, appropriateness and helpfulness of this material and making all medical, diagnostic or prescription decisions.

For questions about the guidelines, CLASP [at] Connecticutchildrens.org (email the CLASP team).