Abstract
We present a case of a 4-month-old infant with abnormal eye movements, unusual flat facies, and lack of expression during crying, clinically diagnosed with Möbius syndrome. MR imaging demonstrated absent facial and abducens nerves. A dysplastic right cerebellar hemisphere containing a cleft and multiple clustered cysts was also observed, which, to our knowledge, represents the first documented case of an association between Möbius syndrome and cerebellar dysplasia. A review of pertinent literature is provided.
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