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- W2000615995 abstract "Chiari malformation type I (CMI) has been considered a sporadic condition without a heritable etiology; however, there have been a number of case reports identifying familial aggregation and clustering of CMI, suggesting a genetic basis [1]. We report two siblings with neuropathic scoliosis (NS) caused by CMI with syringomyelia. The patients and their families were informed that data from the cases would be submitted for publication and gave their consent." @default.
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- W2000615995 date "2015-01-01" @default.
- W2000615995 modified "2023-09-25" @default.
- W2000615995 title "Two siblings with neuropathic scoliosis caused by Chiari malformation type I with syringomyelia" @default.
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- W2000615995 doi "https://doi.org/10.1007/s00776-013-0520-0" @default.
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