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Three different causes of hypercalciuria
S. Skalova, M. Konrad, S. Kutilek,
Language English Country Germany
Document type Case Reports, Journal Article
- MeSH
- Alleles MeSH
- Genetic Carrier Screening MeSH
- Diagnosis, Differential MeSH
- Child MeSH
- Phosphates administration & dosage blood MeSH
- Hypercalciuria diagnosis etiology genetics MeSH
- Claudins genetics MeSH
- Infant MeSH
- Humans MeSH
- Bone Diseases, Metabolic diagnosis MeSH
- DNA Mutational Analysis MeSH
- Follow-Up Studies MeSH
- Nephrocalcinosis diagnosis genetics MeSH
- Infant, Premature, Diseases diagnosis therapy MeSH
- Infant, Low Birth Weight MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Hyperparathyroidism, Secondary diagnosis therapy MeSH
- Calcium urine MeSH
- Renal Tubular Transport, Inborn Errors diagnosis genetics MeSH
- Kidney Function Tests MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
Hypercalciuria is defined as urinary calcium excretion ≥0.1 mmol/kg/24 h, and can be a result of various disease states. The most frequent clinical signs of hypercalciuria include hematuria, abdominal pain, urolithiasis, nephrocalcinosis, dysuria, enuresis, and urinary tract infection. 3 case reports of children with hypercalciuria of different origin are presented, with final diagnoses of (1)idiopathic hypercalciuria, (2)familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), and (3)metabolic bone disease of prematurity, respectively. Assessment of hypercalciuria is essential in all children with urolithiasis and nephrocalcinosis, or demineralization of bone. It should be also a part of differential diagnostic procedure in hematuria, recurrent abdominal pain, urinary tract infection and enuresis in childhood.
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- $a Hypercalciuria is defined as urinary calcium excretion ≥0.1 mmol/kg/24 h, and can be a result of various disease states. The most frequent clinical signs of hypercalciuria include hematuria, abdominal pain, urolithiasis, nephrocalcinosis, dysuria, enuresis, and urinary tract infection. 3 case reports of children with hypercalciuria of different origin are presented, with final diagnoses of (1)idiopathic hypercalciuria, (2)familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), and (3)metabolic bone disease of prematurity, respectively. Assessment of hypercalciuria is essential in all children with urolithiasis and nephrocalcinosis, or demineralization of bone. It should be also a part of differential diagnostic procedure in hematuria, recurrent abdominal pain, urinary tract infection and enuresis in childhood.
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