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To report a case of partial limbal stem cell deficiency and characteristicmucocutaneous triad in an 11-year-old boy. Systemic features along with ocular features are described in this case report. Ophthalmic evaluation showed bilateral partial limbal stem cell deficiency (LSCD) and systemic examination revealed characteristicmucocutaneous triad of oral leukoplakia, skin hypopigmentation, and naildystrophy suggestive of the Zinsser-Engman-Cole syndrome or dyskeratosis congenita. Thorough ocular and systemic evaluation can help in clinch
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