Review Article
Limbal Stem Cell Deficiency: Current Treatment Options and Emerging Therapies
Table 1
Aetiology of LSCD.
| Primary causes | Reference |
| Aniridia | [67, 71, 72] | Multiple endocrine deficiency | [9, 67] | Epidermal dysplasia | | Ectrodactyly-ectodermal-dysplasia-clefting syndrome | [73] | Congenital erythrokeratodermia | [74] | Dyskeratosis congenita | [75, 76] |
| Secondary causes | |
| Thermal or chemical burns | [67, 77] | Contact lens wear | [67, 78] | Inflammatory eye disease: | | Stevens-Johnson syndrome, toxic epidermal necrolysis | [67] | Ocular cicatricial pemphigoid | [79] | Chronic limbitis: autoimmune disease, extensive microbiological infection, atopic conjunctivitis | [80] | Neurotrophic keratitis | [80] | Extensive limbal cryotherapy, radiation, or surgery | [81] | Bullous keratopathy | [82] | Topical antimetabolites (5-FU, Mitomycin C) | [83, 84] | Systemic chemotherapy (Hydroxyurea) | [85] |
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5-FU: 5-fluorouracil.
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