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A Case of McCune-Albright Syndrome with Associated Multiple Endocrinopathies
McCune-Albright syndrome (MAS) is a rare disorder that develops from an activating mutation in the Gs gene. It is characterized by an association with Polyostotic fibrous dysplasia, and precocious puberty, Caf-au-lait pigmentation, and other endocrinopathies that result from the hyperactivity of a v...
| Autores principales: | , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Association of Internal Medicine
2007
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687599/ https://www.ncbi.nlm.nih.gov/pubmed/17427647 http://dx.doi.org/10.3904/kjim.2007.22.1.45 |