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...

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Detalles Bibliográficos
Autores principales: Fantahun, Bereket, Desta, Seblewongel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Case Report
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

Internet

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

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