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vitamin D-resistant rickets, X-linked; X-linked hypophosphatemic rickets
Epidemiology:
- most common form of hypophosphatemia
- incidence of 1 in 20000
Pathology:
- impaired phosphate uptake in the kidney, due to abnormal regulation of Na+ phosphate cotransport in the proximal renal tubules.
Genetics:
- X-linked dominant
- associated with defects in PHEX (phosphate-regulating neutral endopeptidase)
Clinical manifestations:
- skeletal deformities
- growth failure
- craniosynostosis
- paravertebral calcifications
- pseudofractures in lower extremities
- muscular hypotonia with onset in early childhood
Laboratory:
- serum phosphate: hypophosphatemia
- PHEX gene mutation
General
hereditary rickets
Database Correlations
OMIM 307800
References
OMIM :accession 307800