Abstract
We present the imaging findings in a patient with mucopolysaccharidosis (MPS) type VI (Maroteaux-Lamy syndrome) who developed holocord syringomyelia. This represents the only reported case of syrinx formation in a child with MPS VI. Clinical, neurologic and spinal magnetic resonance imaging findings are presented. The patient has maintained a stable clinical and neurologic course over the period following allogeneic bone marrow transplant.
Original language | English (US) |
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Pages (from-to) | 736-738 |
Number of pages | 3 |
Journal | Pediatric Radiology |
Volume | 27 |
Issue number | 9 |
DOIs | |
State | Published - Sep 1997 |