Nischal Ken K

The Oculome Panel Test: Next-Generation Sequencing to Diagnose a Diverse Range of Genetic Developmental Eye Disorders.

The oculome test diagnoses a comprehensive range of genetic conditions affecting the development of the eye, potentially replacing protracted and costly multidisciplinary assessments and allowing for faster targeted management.

Selective Endothelialectomy in Peters Anomaly: A Novel Surgical Technique and Its Clinical Outcomes in Children.

SEPA is a safe and effective technique in select cases of posterior corneal defect due to PA.

Variable Phenotype of Congenital Corneal Opacities in Biallelic CYP1B1 Pathogenic Variants.

Congenital corneal opacities seen in biallelic CYP1B1 pathogenic variants have a variable phenotype.

Glaucoma Management in Sturge-Weber Syndrome Using the Delphi Process.

Consensus for screening, diagnosis, and management in patients with SWS is designed to hopefully improve clinical practice and patient outcomes.

Genetics of Congenital Corneal Opacification--Impact on Diagnosis and Treatment.

Other secondary developmental corneal diseases may include Axenfeld-Rieger syndrome, Aniridia, and primary congenital glaucoma, all of which have specific genotypic characterization. Other secondary causes are acquired and include infection, trauma, and metabolic disorders.

Technique for identifying Schlemm's canal in paediatric glaucoma surgery.