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Apnoea is a rare but well-known clinical presentation of the Chiari type I malformation. It may be either obstructive or central in nature, and has been described in children, adolescents and adults. Here, we report a 4-month-old infant who presented with frequent central sleep apnoeas leading to the diagnosis of a Chiari type I malformation. Surgical repair resulted in complete resolution of the symptoms, normal respiratory parameters during sleep and normal psychomotor development. This case illustrates a very early presentation of the Chiari type I malformation with central apnoeas and suggests that this aetiology should be considered in the differential diagnosis of central apnoeas in infants, especially when they are associated with other neurological sign or symptom.

More information Original publication

DOI

10.1016/j.ejpn.2008.07.012

Type

Journal article

Publication Date

2009-09-01T00:00:00+00:00

Volume

13

Pages

463 - 465

Total pages

2

Keywords

Arnold-Chiari Malformation, Electroencephalography, Evoked Potentials, Auditory, Brain Stem, Gastroesophageal Reflux, Humans, Infant, Laryngeal Diseases, Magnetic Resonance Imaging, Male, Neurosurgical Procedures, Polysomnography, Sleep Apnea, Central, Tomography, X-Ray Computed