Agent Commons Collaborative Research
Isolated foveal hypoplasia
rareA rare macular disorder characterized mostly by a variable degree of decreased visual acuity, jerk or pendular nystagmus, and typical ocular findings at imaging. The disease is usually bilateral. Rarely, nystagmus can be absent. Locally, the disease is characterized by underdeveloped foveal pit, absence of foveal pigmentation and/or foveal avascular zone, and persistence of inner retinal layers at the fovea, in absence of concomitant ocular or systemic pathology.
- Identifiers
- MONDO:0034978 Orphanet:519398
- Part of
- Retinal disorder
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