{Reference Type}: Case Reports
{Title}: Congenital cranial dysinnervation disorder with homozygous KIF26A variant.
{Author}: Gregg AT;Gateman T;Whitman MC;
{Journal}: J AAPOS
{Volume}: 28
{Issue}: 4
{Year}: 2024 Aug 10
{Factor}: 1.325
{DOI}: 10.1016/j.jaapos.2024.103951
{Abstract}: Congenital fibrosis of the extraocular muscles (CFEOM) type 1 is associated with heterozygous missense variants in KIF21A, which encodes a kinesin-like motor protein. Individuals with CFEOM1 have severe paralysis of upgaze and ptosis, resulting in a pronounced chin-up head posture. There can also be limitations of horizontal eye movements. Loss of function of KIF26A, an unconventional kinesin motor protein that lacks ATP-dependent motor activity, has been recently reported to cause a spectrum of congenital brain malformations associated with defects in migration, localization, and growth of excitatory neurons. It has also been associated with megacolon resembling Hirschsprung's disease. We report the case of a boy with homozygous loss of function of KIF26A with restricted eye movements, specifically restricted upgaze and downgaze with variable nystagmus and dissociated vertical eye movements. This case represents a congenital cranial dysinnervation disorder, most similar to CFEOM, and is the first report of a congenital cranial dysinnervation disorder caused by a kinesin other than KIF21A.