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Axenfeld-Reiger syndrome: A search for the missing links

World Journal of Clinical Cases 2023年第29期11卷 7034-7042页

作者： Arvind Kumar Morya Prasanna Venkatesh Ramesh Sony Sinha Prateek Nishant Nazia Nain Ravi NaikRamavath Chetana Gone Ripunjay Prasad Department of Ophthalmology All India Institute of Medical SciencesBibi NagarHyderabad 508126TelanganaIndia Glaucoma Medical Officer Mahathma Eye Hospital Private LimitedThennurTrichy 620017Tamil NaduIndia Department of Ophthalmology-Vitreo-Retina and Oculoplasty All India Institute of Medical SciencesPatnaPatna 801507BiharIndia Department of Ophthalmology All India Institute of Medical SciencesPatnaPatna 801507BiharIndia Department of Ophthalmology RP Eye InstituteDelhi 110001DelhiIndia

BACKGROUND Axenfeld-Rieger syndrome(ARS)is a rare cause of congenital glaucoma and may result in loss of *** is mostly autosomal dominant in nature characterized by developmental abnormalities in the angle of anterior chamber and iris of the eye,also associated with structural abnormalities in the *** To study and observe the demographics and clinical findings in a very rare ocular disease known as *** Case records of symptomatic patients attending Ophthalmology outpatient department and diagnosed to have ocular hypertension or glaucoma in 3 years from March 2017 to March 2020 were evaluated to search for cases diagnosed with *** of all patients diagnosed with ARS were then analysed for demographic and clinical characterization as well as management and success of *** Eight out of ten patients with positive clinical signs were symptomatic and had *** of these patients had limbal stem cell deficiency and another had vernal *** Clinical characterization of ARS is important for making a definitive diagnosis and determining prognosis.

关键词： Axenfeld-Reiger Syndrome Glaucoma Limbal stem cell deficiency vernal keratoconjuctivitis

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