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McCune-Albright Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that McCune-Albright Syndrome, or a subtype of McCune-Albright Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list McCune-Albright Syndrome as a "rare disease".
Source - Orphanet
McCune-Albright Syndrome: Introduction
Broader types of McCune-Albright Syndrome:
Patient Profile for McCune-Albright Syndrome: Congenital disease starting at birth.
Complications of McCune-Albright Syndrome:
see complications of McCune-Albright Syndrome
Causes of McCune-Albright Syndrome: see causes of McCune-Albright Syndrome
Symptoms of McCune-Albright Syndrome: see symptoms of McCune-Albright Syndrome
Complications of McCune-Albright Syndrome: see complications of McCune-Albright Syndrome
Diagnostic testing: see tests for McCune-Albright Syndrome.
Misdiagnosis: see misdiagnosis and McCune-Albright Syndrome.
Treatments for McCune-Albright Syndrome:
see treatments for McCune-Albright Syndrome
Research for McCune-Albright Syndrome:
see research for McCune-Albright Syndrome
Organs and body systems related to McCune-Albright Syndrome include:
Main name of condition: McCune-Albright Syndrome
Other names or spellings for McCune-Albright Syndrome:osteitis gibrosa cystica, MAS, Albright syndrome, Polyostotic fibrous dysplasia, PFD, POFD, Sexual precocity, familial, gonadotropin-independent, female-limited
Polyostotic fibrous dysplasia
Source - Diseases Database
Albright syndrome, MAS, PFD, POFD, Polyostotic fibrous dysplasia
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Research the causes of these diseases that are similar to, or related to, McCune-Albright Syndrome:
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