Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis
Ectodermal malformation syndrome associated with ocular features +
Familial amyloidosis, Finnish type
Fuchs endothelial corneal dystrophy
Genetic developmental defect of the eye +
Genetic lens and zonula anomaly +
Genetic neuro-ophthalmological disease +
Genetic vitreous-retinal disease +
Genodermatosis with ocular features +
keratitis +
keratoconus +
megalocornea +
Metabolic disease associated with ocular features +
Microcystic corneal dystrophy
Optic neuropathy +
Peters anomaly +
Rare disease with glaucoma as a major feature +
Rare genetic palpebral, lacrimal system and conjunctival disease +
Rare genetic refraction anomaly +
Reis-Bücklers corneal dystrophy
Reis-Bücklers corneal dystrophy (RBCD), also known as granular corneal dystrophy type III, is a rare form of superficial corneal dystrophy characterized by bilateral symmetrical reticular opacities in the superficial central cornea, with progressive visual impairment.
sclerocornea +
Spastic ataxia - corneal dystrophy
Subaortic stenosis - short stature
X-linked corneal dermoid
X-linked reticulate pigmentary disorder with systemic manifestations
Synonyms
Exact Synonyms:
Anterior limiting membrane dystrophy type I
;
Atypical granular corneal dystrophy
;
Corneal dystrophy of Bowman layer type I
;
Geographic corneal dystrophy
;
Granular corneal dystrophy type III
;
RBCD
;
Superficial granular corneal dystrophy