Abstract
Mutations of the CYP24A1 gene, encoding for the enzyme 25(OH)D-24-hydroxylase, can cause hypercalcemia, hypercalciuria, nephrolithiasis and nephrocalcinosis. We report the case of a 22-year-old male patient with recurrent nephrolithiasis, nephrocalcinosis, hypercalcemia with low parathyroid hormone levels, hypercalciuria and low bone mass. Gene sequencing showed that the patient had compound heterozygous mutations including a novel genotype of the CYP24A1 gene. Genetic CYP24A1 testing and biochemical analyses were offered to other family members; the father was heterozygous for the same novel genotype and was also affected with recurrent nephrolithiasis.
Lingua originale | English |
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pagine (da-a) | 295-294 |
Numero di pagine | 4 |
Rivista | Urolithiasis |
Volume | 45 |
DOI | |
Stato di pubblicazione | Pubblicato - 2017 |
Keywords
- Genetics
- Hypercalciuria
- Osteoporosis
- Urolithiasis
- Vitamin D