Pamidronic acid and cabergoline as effective long-term therapy in a 12-year-old girl with extended facial polyostotic fibrous dysplasia, prolactinoma and acromegaly in McCune-Albright syndrome: a case report

INTRODUCTION: McCune-Albright syndrome is a complex inborn disorder due to early embryonal postzygotic somatic activating mutations in the GNAS1 gene. The phenotype is very heterogeneous and includes polyostotic fibrous dysplasia, typically involving the facial skull, numerous café-au-lait spots and...

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Detalles Bibliográficos
Autores principales: Classen, Carl Friedrich, Mix, Monika, Kyank, Ulrike, Hauenstein, Christina, Haffner, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277484/
https://www.ncbi.nlm.nih.gov/pubmed/22273876
http://dx.doi.org/10.1186/1752-1947-6-32

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277484/
https://www.ncbi.nlm.nih.gov/pubmed/22273876
http://dx.doi.org/10.1186/1752-1947-6-32

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