Mild Oculocutaneous Albinism Type 1B With Subtle Cutaneous Findings: A Dermatology-Oriented Case Report

variants consistent with OCA1B, followed by genetic counseling regarding autosomal recessive inheritance. Dermatologic evaluation later revealed Fitzpatrick phototype II skin and gray-green irides consistent with a mild hypopigmented phenotype of OCA1B. Mild acneiform lesions were also observed and considered incidental findings. This case highlights the importance of dermatologic assessment within a multidisciplinary diagnostic pathway, contributing to the recognition of subtle cutaneous phenotypes and the implementation of long-term photoprotection and surveillance strategies in patients with mild albinism.