I present a review of the pattern of rare craniofacial clefting in pat
ients presenting to a tertiary referral craniofacial unit. Patients wi
th an isolated rare cleft were uncommon; most had multiple axes of dis
ruption. Midline and paramedian facial clefts, although occasionally o
ccurring alone, often overlap with adjacent facial clefts and extend a
long an upward cranial axis. The corresponding midline and paramedian
facial clefts were never seen in isolation but were almost always seen
with their axial downward cleft, Lateral nasal, oro-ocular, and later
al forehead clefts showed diffuse and often poorly defined regions of
disruption, resulting in a multiplicity in clefts. The small subgroup
of patients with features of the amniotic band sequence had more and d
ifferently distributed clefts compared with the larger nonamniotic ban
d group.