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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Autors principals: Hirohata, Toshio, Miyawaki, Satoru, Mizutani, Akiko, Iwakami, Takayuki, Yamada, So, Nishido, Hajime, Suzuki, Yasutaka, Miyamoto, Shinya, Hoya, Katsumi, Murakami, Mineko, Matsuno, Akira
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2014
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4131488/
https://ncbi.nlm.nih.gov/pubmed/25056440
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2377-14-150
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