Horseshoe kidney is a congenital disorder, distressing roughly 1 in 400 people, in which a person's two kidneys fuse jointly to develop a horseshoe-shape throughout progress in the womb.
A horseshoe kidney is notable due to its atypical location, its unusual orientation, its abnormal blood supply, and the problematical placement of the ureters into it.
All of this could cause a higher risk of kidney disease and complications.
Horseshoes kidneys don't typically lead to symptoms by themselves.
But, medical conditions or complications related with them could bring about substantial symptoms.
For a lot of people, by the way they are found through a radiology test completed for another reason or on autopsy.
Treatment for the horseshoe kidney itself is contentious and not typically revealed.
As an alternative, treatment is typically aimed at the complications produced by it.
Horseshoe kidney has been informed to be related with increased risk for renal neoplasms, like Wilms tumors, renal carcinoids, and transitional cell carcinoma.
People affected by this disease can feel nausea, abdominal distress, kidney stones and urinary tract infections.
In a child with no symptoms, treatment may not be needed.
If your child has complications, he/she might need supportive treatment, which means his/her symptoms will be treated, but there is no cure for the circumstance.
Exact treatment for horseshoe kidney will be decided by your child's physician rooted in your child's age, overall health, and medical history; the extent of the disorder, your child's broadmindedness for certain medications, procedures, or therapies, hopes for the course of the disorder, your judgment or preference.
Your child can be checked to an urologist and/or a nephrologist for evaluation.