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- W2012609099 abstract "<h3>To the Editor.</h3> —It has been reported that syringobulbia rarely, if ever, occurs in the absence of syringomyelia.<sup>1,2</sup>Using high-resolution computed tomographic (CT) scans, we recently examined a man with a gradually progressive spastic quadriparesis and segmental bulbar signs who we believe had this rarely reported condition. <h3>Report of a Case.</h3> —A 59-year-old man had had gradually progressive spastic quadriparesis for 20 years and urinary incontinence for 15 years. There was no personal or family history of headache, neck pain, optic neuritis, diplopia, dysphagia, or dysarthria. On examination, he was alert and oriented, with normal higher intellectual functions. Funduscopic findings and visual fields were normal. The right pupil was 5 mm in diameter, the left pupil was 4 mm in diameter, and both were briskly reactive to light. There was no ptosis. The extraocular movements were normal, as was facial sensation. The right nasolabial fold was very slightly" @default.
- W2012609099 created "2016-06-24" @default.
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- W2012609099 date "1983-06-01" @default.
- W2012609099 modified "2023-10-06" @default.
- W2012609099 title "Syringobulbia Without Syringomyelia" @default.
- W2012609099 cites W1988107669 @default.
- W2012609099 cites W1994186835 @default.
- W2012609099 doi "https://doi.org/10.1001/archneur.1983.04050060094032" @default.
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