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Delayed Diagnosis of McCune–Albright Syndrome
BACKGROUND: McCune–Albright syndrome (MAS) is a rare heterogeneous genetic disorder that is characterized by a triad of polyostotic fibrous dysplasia (FD), café au lait spots (CAL), and multiple hyperfunctional endocrinopathies. In general, it is diagnosed clinically. From the triads, two of the fin...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683245/ https://www.ncbi.nlm.nih.gov/pubmed/34925926 http://dx.doi.org/10.1155/2021/2999349 |