Aims: This study reports a case of localized ocular surface squamous neoplasia (OSSN) and highlights the role of anterior segment optical coherence tomography (AS-OCT) in diagnosis, surgical planning, and postoperative surveillance. Presentation of Case: A 60-year-old male farmer...
Open access
Research Article10.9734/or/2026/v21i1494
Autosomal Recessive Congenital Ichthyosis (ARCI) is a heterogeneous group of inherited disorders of cornification, with CERS3 mutations being a rare cause that typically produces a lamellar ichthyosis–like phenotype due to defective synthesis of very long-chain ceramides essentia...
Open access
Research Article10.9734/ajrrop/2026/v9i1139
Bardet-Biedl Syndrome (BBS) is a rare autosomal recessive ciliopathy with multisystem involvement. We present the case of a 7-year-old boy who presented with photophobia and difficulty seeing in dim light. Examination revealed central obesity, bilateral post-axial polydactyly of...
Open access
Research Article10.9734/or/2025/v20i5471