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Peculiarities of Precocious Puberty in Boys and Girls With McCune-Albright Syndrome
McCune-Albright Syndrome (MAS; OMIM # 174800) is a rare, sporadic disease caused by a post-zygotic, activating mutation in the guanine-nucleotide binding protein α-subunit (GNAS1) gene. MAS is characterized by the clinical triad of polyostotic fibrous dysplasia of bone, café-au-lait skin pigmentatio...
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| Veröffentlicht in: | Front Endocrinol (Lausanne) |
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| Hauptverfasser: | , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Frontiers Media S.A.
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6023984/ https://ncbi.nlm.nih.gov/pubmed/29988390 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2018.00337 |
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