[1] The disorder is characterized by the following:[1] Individuals with Albright hereditary osteodystrophy exhibit short stature, characteristically shortened fourth and fifth metacarpals, rounded facies, and often mild intellectual deficiency.

It is thought to be inherited in an autosomal dominant pattern, and seems to be associated with a Gs alpha subunit deficiency.

Renal tubule cells only express maternal alleles (variant form of a gene).

[6][7][8] The diagnosis of Albright's hereditary osteodystrophy is based on the following exams below:[9] Treatment consists of maintaining normal levels of calcium, phosphorus, and vitamin D. Phosphate binders, supplementary calcium and vitamin D will be used as required.

[13] This article incorporates text in the public domain from page 798 of the 20th edition of Gray's Anatomy (1918)