Albright's hereditary osteodystrophy
| Albright's hereditary osteodystrophy | |
|---|---|
| Albright's hereditary osteodystrophy has an autosomal dominant pattern of inheritance | |
| Specialty | Endocrinology | 
| Symptoms | Choroid plexus calcification, Full cheeks | 
| Causes | Gs alpha subunit deficiency | 
| Diagnostic method | calcium, phosphorus, PTH, Urine test for phosphorus and cyclic AMP | 
| Treatment | Phosphate binders, supplementary calcium | 
| Named after | Fuller Albright | 
Albright's hereditary osteodystrophy is a form of osteodystrophy, and is classified as the phenotype of pseudohypoparathyroidism type 1A; this is a condition in which the body does not respond to parathyroid hormone.