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  2. McCune–Albright syndrome - Wikipedia

    en.wikipedia.org/wiki/McCuneAlbright_syndrome

    McCune–Albright syndrome is a complex genetic disorder affecting the bone, skin and endocrine systems. It is a mosaic disease arising from somatic activating mutations in GNAS , which encodes the alpha-subunit of the G s heterotrimeric G protein .

  3. Albright's hereditary osteodystrophy - Wikipedia

    en.wikipedia.org/wiki/Albright's_hereditary...

    The disorder bears the name of Fuller Albright, who characterized it in 1942. [12] He was also responsible for naming it "Sebright bantam syndrome," after the Sebright bantam chicken, which demonstrates an analogous hormone insensitivity. Much less commonly, the term Martin-Albright syndrome is used, this refers to Eric Martin. [13]

  4. Fibrous dysplasia of bone - Wikipedia

    en.wikipedia.org/wiki/Fibrous_dysplasia_of_bone

    Managing endocrinopathies is a critical component of management in FD. All patients with fibrous dysplasia should be evaluated and treated for endocrine diseases associated with McCune–Albright syndrome. In particular untreated growth hormone excess may worsen craniofacial fibrous dysplasia and increase the risk of blindness. [23]

  5. Multiple endocrine neoplasia - Wikipedia

    en.wikipedia.org/wiki/Multiple_endocrine_neoplasia

    Multiple Endocrine Neoplasia type 1 (MEN1) is a rare hereditary endocrine cancer syndrome characterized primarily by tumors of the parathyroid glands (95% of cases), endocrine gastroenteropancreatic (GEP) tract (30–80% of cases), and anterior pituitary (15–90% of cases). [19]

  6. Café au lait spot - Wikipedia

    en.wikipedia.org/wiki/Café_au_lait_spot

    Café au lait spots are often harmless but may be associated with syndromes such as neurofibromatosis type 1 and McCune–Albright syndrome. [3] Café au lait lesions with rough borders ("coast of Maine") may be seen in McCune–Albright syndrome.

  7. Spondyloepiphyseal dysplasia congenita - Wikipedia

    en.wikipedia.org/wiki/Spondyloepiphyseal...

    Spondyloepiphyseal dysplasia congenita (abbreviated to SED more often than SDC) is a rare disorder of bone growth that results in dwarfism, [1] characteristic skeletal abnormalities, and, in some instances, problems with vision and hearing.

  8. Michael Levine (physician) - Wikipedia

    en.wikipedia.org/wiki/Michael_Levine_(physician)

    Moreover, he also worked on identifying a gain-of-function mutation in the GNAS gene as the basis for constitutive activation of adenylyl cyclase in the McCune-Albright syndrome and confirmed that the unusual distribution of the endocrine, cutaneous, and skeletal lesions in the syndrome is the result of a postzygotic mosaicism. [9]

  9. Donovan James McCune - Wikipedia

    en.wikipedia.org/wiki/Donovan_James_McCune

    Donovan James McCune (June 24, 1902 – April 11, 1976) was an American pediatrician who conducted pioneering research on McCune–Albright syndrome. [1] He was also a collector of rare books, including many incunabula , and a devotee of letterpress printing .