Abstract : We report a rare case of a five-year-old female child who was diagnosed with Miller-Dieker syndrome.
She had global developmental delay, seizures, facial dysmorphic features and type 1 lissencephaly on
Magnetic resonance imaging of brain. Her ocular manifestations included strabismus, torsional nystagmus,
high myopic astigmatism and tortuous retinal vessels.
Keywords: Miller- dieker syndrome, Dysmorphism, Lissencephaly, Nystagmus, Strabismus.