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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...
Autores principales: | Hirohata, Toshio, Miyawaki, Satoru, Mizutani, Akiko, Iwakami, Takayuki, Yamada, So, Nishido, Hajime, Suzuki, Yasutaka, Miyamoto, Shinya, Hoya, Katsumi, Murakami, Mineko, Matsuno, Akira |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
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 |
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