Syringohydromyelia in Hajdu-Cheney syndrome. [Pediatr Radiol. 1996]

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1: Pediatr Radiol. 1996;26(1):59-61.Links

Syringohydromyelia in Hajdu-Cheney syndrome.

Nishimura G, Aoki K, Haga N, Hasegawa T.

Department of Radiology, Dokkyo University School of Medicine, Kitakobayashi, Mibu, Shimotuga-gun, Tochigi-ken 321-02, Japan.

We report the case of a 10-year-old boy with typical manifestation of Hajdu-Cheney syndrome. MRI demonstrated syringohydromyelia involving almost the entire spinal cord, although neurological symptoms had not yet developed. Syringohydromyelia is considered to be a sequel to progressive basilar invagination and is one of the essential features of this rare osteolytic bone dysplasia.

PMID: 8598999 [PubMed - indexed for MEDLINE]

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ReviewThe Hajdu-Cheney syndrome: a case report and review of the literature. [Pediatr Radiol. 1990]

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Syringohydromyelia in Hajdu-Cheney syndrome.

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