Neonatal McCune–Albright syndrome with systemic involvement: a case report

INTRODUCTION: McCune–Albright syndrome is a rare sporadic disease characterized by fibrous bone dysplasia, café-au-lait skin spots and variable hyperfunctional endocrinopathies. McCune–Albright syndrome is caused by somatic postzygotic activating mutations in the GNAS gene that produce a broad spect...

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Detalles Bibliográficos
Autores principales: Lourenço, Rita, Dias, Patrícia, Gouveia, Raquel, Sousa, Ana Berta, Oliveira, Graça
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560899/
https://www.ncbi.nlm.nih.gov/pubmed/26341786
http://dx.doi.org/10.1186/s13256-015-0689-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560899/
https://www.ncbi.nlm.nih.gov/pubmed/26341786
http://dx.doi.org/10.1186/s13256-015-0689-2

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