Familial hemiplegic migraine (FHM) is an autosomal dominant syndrome c
haracterized by recurrent episodes of varying degrees of hemiparesis a
ssociated with migraine. The aura including hemiparesis may be prolong
ed and in severe attacks may often be associated with confusion or com
a, We describe a case of FHM whose aura was atypically prolonged and r
esulted in irreversible brain deficit which on magnetic resonance imag
ing (MRI) was suggestive of cortical hyperperfusion. A subsequent MRI
showed left brain atrophy.