Hereditary / Congenital | Columbia Ophthalmology

X-linked juvenile retinoschisis is characterized by splitting of the superficial layers of the sensory retina. Most cases demonstrate a stellate or spoke wheel-like maculopathy. Bilateral microcystic-like changes of the macula are shown in OCT studies.

Bietti's Crystalline Retinopathy
Optic Disc Pit
Optic Disc Pit
Myelinated Fibers
X-linked Juvenile Retinoschisis
Chorioretinal Coloboma
Optic Disc Pit (OCT Study)
Myelinated Fibers
Prepapillary Vascular Loops
X-linked Juvenile Retinoschisis (OCT Study)