Rare coexistence of hypopituitarism with osteogenesis imperfecta – A double-trouble for bone

Osteogenesis imperfecta (OI) commonly involving defects in COL1A1 and COL1A2 is a rare hereditary disease of bone fragility affecting 6–7 per 100,000 population. On the other hand, hypopituitarism is a separate entity that manifests with reduced levels of pituitary hormones. The cooccurrence of thes...

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Detalhes bibliográficos

Principais autores:	Rajdeep Basu, Soumik Goswami, Nilanjan Sengupta, Arjun Baidya, Sunetra Mondal, Kumar Swapnil, Rajat Deb, Vibhu Ranjan Khare, Joydip Datta
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Elsevier 2024-06-01
coleção:	Bone Reports
Assuntos:	Pathological fracture Hypopituitarism Osteogenesis imperfecta
Acesso em linha:	http://www.sciencedirect.com/science/article/pii/S2352187224000354
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