Skip to
  1. Homepage
  2. Rare diseases
  3. Search
PrintPrint
Simple search

Simple search

*
(*) mandatory field





Other search option(s)

Horseshoe kidney

Orpha number ORPHA3029
Prevalence of rare diseases >1 / 1000
Inheritance -
Age of onset Variable
ICD 10 code
  • Q63.1
MIM number -
Synonym(s) -

Summary

Horseshoe kidney is the most frequent renal fusion anomaly and is characterised by the union of the inferior poles of the two kidneys through an isthmus. The incidence at birth varies between 1 in 400 and 1 in 800: it is therefore not a rare condition. Horseshoe kidney is in fact a anatomical anomaly rather than a disease, but it does lead to predisposition to certain conditions such as hydronephrosis, nephrolithiasis or pyelonephritis. One third of individuals with horseshoe kidney are asymptomatic, with the anomaly being discovered fortuitously during a radiological examination. Urogenital or renal vessel anomalies may be associated with the condition. For cases requiring treatment, various therapeutic approaches (surgery or medication) are available and choice of treatment depends on the associated pathology. *Author: Orphanet (March 2006)*.

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Languages :