Axenfeld-Rieger syndrome diagnosed in adulthood: A case report
Author(s): Miguel Angel Herrero Delicado
Abstract: Axenfeld-Rieger Syndrome is a rare congenital disorder that affects the anterior segment of the eye and is often accompanied by systemic anomalies. Although it is typically diagnosed in childhood, some cases go undetected until adulthood, particularly when the ocular phenotype is subtle and glaucoma develops later. We report a case of a 40-year-old male diagnosed with Axenfeld-Rieger Syndrome, emphasizing the ocular and systemic findings, diagnostic challenges, and management strategies. This case also underscores the importance of genetic counseling, as it can provide crucial information and support to patients and their families, helping them understand the genetic basis of the syndrome and make informed decisions about their offspring’s health.
Miguel Angel Herrero Delicado. Axenfeld-Rieger syndrome diagnosed in adulthood: A case report. Int J Med Ophthalmol 2025;7(1):59-63. DOI: 10.33545/26638266.2025.v7.i1a.225
