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Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?

BACKGROUND: Osteochondroma generally occurs as a single lesion and it is not a heritable disease. When two or more osteochondroma are present, this condition represents a genetic disorder named hereditary multiple exostoses (HME). Growth hormone deficiency (GHD) has rarely been found in HME patients...

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Detalles Bibliográficos
Autores principales:	Bozzola, Mauro, Gertosio, Chiara, Gnoli, Maria, Baronio, Federico, Pedrini, Elena, Meazza, Cristina, Sangiorgi, Luca
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4524199/ https://www.ncbi.nlm.nih.gov/pubmed/26239617 http://dx.doi.org/10.1186/s13052-015-0162-2

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