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endocrine, genetic or congenital
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rare (U.S.)
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Definition for McCune-Albright Syndrome

McCune-Albright syndrome (polyostotic fibrous dysplasia), described in 1937 by Donovan James McCune and Fuller Albright, is a genetic disorder of bones, skin pigmentation and hormonal problems along with premature puberty. more


some common symptoms
increased skin pigmentation
leg length discrepancy
pain in bone(s)
rash


some related diagnoses
1 - 7 of 16 diagnoses
multiple endocrine neoplasia type 1
multiple endocrine neoplasia type 2b
trauma
drugs and toxins
malnutrition
celiac disease
sarcoidosis
  more

do i have 'McCune-Albright Syndrome'?
In addition the following diagnostic tests might be need to help verify the diagnosis:
diagnostic test search results for 'mccune-albright syndrome'
1 - 5 of 33 diagnostic tests
X-rays
Leuteinizing hormone (LH)
Serum Testosterone
Serum calcium
Serum phosphorus
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therapeutic procedures for 'McCune-Albright Syndrome'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for McCune-Albright Syndrome:


medications search results for 'mccune-albright syndrome'
1 - 5 of 23 medications
rankings are computer generated. please consult your health care provider.
  vitamin D
  hormone replacement therapy
  serum calcium
  tamoxifen
  Testolactone
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web search results for mccune-albright syndrome
Results 1 - 50 - McCune-Albright Syndrome
adam.about.com - summary
en.wikipedia.org - summary
ghr.nlm.nih.gov - summary
my.clevelandclinic.org - summary
health.yahoo.com - summary
www.ncbi.nlm.nih.gov - summary







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