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20q13.2 Google OMIM Orphanet PubMed Who named it? Wikipedia [Histology] [Imaging] McCune-Albright syndrome *Gene map locus 20q13.2 Albright syndrome MAS PFD Polyostotic fibrous dysplasia [Clinical features: polyostotic fibrous dysplasia; cafe-au-lait spots; precocious puberty; hyperthyroidism] [Inheritance: somatic mosaicism] |
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MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: a case report |
Albright Syndrome |
McCune-Albright Syndrome |
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Cases Journal |
eMedicine |
eMedicine |
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McCune Albright syndrome (MCAS): a case series |
McCune-Albright syndrome |
McCune-Albright syndrome |
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Indian Pediatrics |
Orphanet Journal of Rare Diseases |
Orphanet Journal of Rare Diseases |
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Edited by Aldo Campana,
August 21, 2012
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