4.1 Article

LEOPARD Syndrome and Chiari Type I Malformation A Case Report and Review of the Literature

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NEUROLOGIST
卷 15, 期 1, 页码 37-39

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/NRL.0b013e31817833c4

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LEOPARD syndrome; Noonan syndrome; Chiari type I malformation (CM-1); dysphagia; syringomyelia; percutaneous endoscopic gastrostomy (PEG) tube

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Introduction: The authors present a 31-year-old man with a Chiari type I malformation (CM-1) occurring in conjunction with LEOPARD syndrome. He presented with severe dysphagia requiring placement of a percutaneous endoscopic gastrostomy (PEG) tube. Evaluation included magnetic resonance imaging (MRI) of the brain and cervical spine that revealed CM-1 with an extensive cervical syrinx. The patient underwent a suboccipital craniectomy with C1 laminectomy and duraplasty. His symptoms quickly resolved and his PEG tube was removed. Discussion: The occurrence of a CM-1 with LEOPARD syndrome has only been reported once, whereas CM-1 and Noonan syndrome have been linked in several cases. The similarity between LEOPARD and Noonan syndromes has been reported and many propose they represent 2 entities along a spectrum. Conclusion: In light of this spectrum, we propose that CM-1 should be considered in all patients presenting with LEOPARD-Noonan syndrome.

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