McCune-Albright syndrome

McCune-Albright syndrome
ICD-10	Q78.1
ICD-9	756.54
OMIM	174800
DiseasesDB	7880
MedlinePlus	001217
eMedicine	ped/1386
MeSH	D005359

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

McCune-Albright syndrome is a rare genetic disorder caused by an activating mutation of the GNAS gene resulting in various phenotypic presentations. MAS typically presents with the triad of polyostotic fibrous dysplasia, precocious puberty and café au lait spots in both genders. Other manifestations include hyperthyroidism, acromegaly and Cushing’s syndrome.

See also

• Fibrous dysplasia

External links

• Medterms.com
• GNAS gene
• NORD