Migraine is currently considered
to be a multifactorial disease
in that it is modified by environmental
and genetic factors and has a
polygenic determination. Familial
hemiplegic migraine (FHM), a subtype
of migraine with aura conforming
to simple mendelian transmission,
has been shown to result from
mutations in the CACNA1A gene, a
neural calcium channel gene. FHM
is allelic with episodic ataxia type 2
and spinocerebellar ataxia type 6.
FHM is genetically heterogeneous,
with at least another linkage locus
on chromosome 1. Association and
linkage studies have also been performed
in migraine with and without
aura, the so–called typical migraines,
without however definite results up
to now.