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.