Hypophosphatemic Rickets in Norway

Status Active, not recruiting

Clinical Trial Summary

The purpose of the study is to do a follow-up survey of all individuals with hereditary hypophosphatemia in Norway, focusing on manifestations in childhood and adolescence. The investigators also want to study phenotype-genotype associations, and look for new genes, in all forms of hereditary hypo and hyperphosphatemia.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01057186
Study type	Observational
Source	Haukeland University Hospital
Contact
Status	Active, not recruiting
Phase	N/A
Start date	December 2009

View Details

See also
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