McCune-Albright Syndrome in Infant with Growth Hormone Excess

Background: McCune-Albright is a rare syndrome, caused by mutation of the GNAS1 gene, and is characterized by an appearance of multiple endocrinopathies, most commonly premature puberty, polyostotic fibrous dysplasia and skin changes called cafe au lait macules. Case report: We present the case of a...

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Detalles Bibliográficos
Autores principales: Brzica, Katarina, Simunovic, Marko, Ivancic, Matea, Tudor, Darija, Skrabic, Ivna, Skrabic, Veselin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407244/
https://www.ncbi.nlm.nih.gov/pubmed/36011254
http://dx.doi.org/10.3390/genes13081345

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407244/
https://www.ncbi.nlm.nih.gov/pubmed/36011254
http://dx.doi.org/10.3390/genes13081345

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