Serum phosphate concentrations are regulated by a complex and poorly understood process. Insight into this process can be obtained by analysis of genetic aberrations in phosphate homeostasis. Autosomal dominant hypophosphatemic rickets (ADHR) is an inherited disorder characterized by renal phosphate wasting and consequent hypophosphatemia that results in severe bone pain, fracture, lower extremity deformity, and short stature in affected individuals. The etiology of the phosphate wasting defect is unknown. The ADHR gene locus has been mapped to chromosome 12p13 and the goal of our study is to identify the gene responsible for the disorder using positional cloning techniques.
The specific aims proposed to attain this goal are: 1) To narrow the ADHR region using linkage analysis and deletion analysis of DNA from affected individuals; 2) To identify candidate genes within the ADHR interval; and 3) To identify the ADHR gene by detecting a disease specific alteration in one of these candidates. Identification of the gene will provide insight into the control of phosphate homeostasis and lead to an improved understanding of the pathogenesis of this disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AR008550-02
Application #
6352143
Study Section
General Medicine B Study Section (GMB)
Program Officer
Mcgowan, Joan A
Project Start
2000-08-01
Project End
Budget Start
2000-08-01
Budget End
2001-07-31
Support Year
2
Fiscal Year
2000
Total Cost
$39,232
Indirect Cost
Name
Indiana University-Purdue University at Indianapolis
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005436803
City
Indianapolis
State
IN
Country
United States
Zip Code
46202
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