Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Book

Albright Hereditary Osteodystrophy

In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan.
.
Affiliations
Free Books & Documents
Book

Albright Hereditary Osteodystrophy

Vijaya Sarathi et al.
Free Books & Documents

Excerpt

Albright hereditary osteodystrophy (AHO) phenotype was first described in 1942 by Fuller Albright. AHO refers to a constellation of signs, including a round face, short stature with a stocky habitus, brachydactyly, subcutaneous ossification, and dental anomalies. Developmental delay, obesity (early-onset), and relative macrocephaly may be the additional features of AHO.

PubMed Disclaimer

Conflict of interest statement

Disclosure: Vijaya Sarathi declares no relevant financial relationships with ineligible companies.

Disclosure: Roopma Wadhwa declares no relevant financial relationships with ineligible companies.

References

    1. MACGREGOR ME, WHITEHEAD TP. Pseudo-hypoparathyroidism; a description of three cases and a critical appraisal of earlier accounts of the disease. Arch Dis Child. 1954 Oct;29(147):398-418. - PMC - PubMed
    1. Mantovani G, Elli FM. Inactivating PTH/PTHrP Signaling Disorders. Front Horm Res. 2019;51:147-159. - PubMed
    1. Mouallem M, Shaharabany M, Weintrob N, Shalitin S, Nagelberg N, Shapira H, Zadik Z, Farfel Z. Cognitive impairment is prevalent in pseudohypoparathyroidism type Ia, but not in pseudopseudohypoparathyroidism: possible cerebral imprinting of Gsalpha. Clin Endocrinol (Oxf) 2008 Feb;68(2):233-9. - PubMed
    1. Wilson LC, Trembath RC. Albright's hereditary osteodystrophy. J Med Genet. 1994 Oct;31(10):779-84. - PMC - PubMed
    1. Wilson LC, Hall CM. Albright's hereditary osteodystrophy and pseudohypoparathyroidism. Semin Musculoskelet Radiol. 2002 Dec;6(4):273-83. - PubMed

Publication types

LinkOut - more resources