Subarachnoid hemorrhage secondary to a ruptured middle cerebral aneurysm in a patient with osteogenesis imperfecta: a case report

BACKGROUND: Osteogenesis imperfecta (OI) is a heterogeneous group of inherited disorders that occur owing to the abnormalities in type 1 collagen, and is characterized by increased bone fragility and other extraskeletal manifestations. We report the case of a patient who was diagnosed with OI follow...

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Detalles Bibliográficos
Autores principales: Hirohata, Toshio, Miyawaki, Satoru, Mizutani, Akiko, Iwakami, Takayuki, Yamada, So, Nishido, Hajime, Suzuki, Yasutaka, Miyamoto, Shinya, Hoya, Katsumi, Murakami, Mineko, Matsuno, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131488/
https://www.ncbi.nlm.nih.gov/pubmed/25056440
http://dx.doi.org/10.1186/1471-2377-14-150

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131488/
https://www.ncbi.nlm.nih.gov/pubmed/25056440
http://dx.doi.org/10.1186/1471-2377-14-150

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