Accidentally detected nephrocalcinosis in a boy with a homozygous R396W mutation in the CYP24A1 gene - 7-year follow-up
Nephrocalcinosis can manifest as frequent urination, haematuria and recurrent urinary tract infections, as well as a decrease in bone mineral density, increasing the risk of osteoporosis. Excessive urinary calcium excretion may have a genetic basis, including mutations within the genes encoding vita...
Saved in:
| Main Authors: | , , , , |
|---|---|
| Format: | Book |
| Published: |
Termedia Publishing House,
2023-12-01T00:00:00Z.
|
| Subjects: | |
| Online Access: | Connect to this object online. |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|