Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?
作者： Mauro Bozzola , Chiara Gertosio , Maria Gnoli , Federico Baronio , Elena Pedrini
DOI: 10.1186/S13052-015-0162-2
关键词: Disease 、 Growth hormone deficiency 、 Osteochondroma 、 Genetic disorder 、 Multiple exostosis 、 Pathology 、 Single lesion 、 Hereditary multiple exostoses 、 Medicine 、 Solitary Osteochondroma
摘要: Background Osteochondroma generally occurs as a single lesion and it is not heritable disease. When two or more osteochondroma are present, this condition represents genetic disorder named hereditary multiple exostoses (HME). Growth hormone deficiency (GHD) has rarely been found in HME patients few data about growth therapy (GH) effects development/growth of solitary have reported.
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