Stargardt Disease a Clinical Finding of Circumb Papillary Band Shape Hyperpigmentery Hallow

Department of Ophthalmology, Razi Hospital, Ghafari St, Birjand University of Medical Sciences, Birjand, Iran

*Corresponding Author: Dr. Gholamhossein Yaghoobi, Department of Ophthalmology, Razi Hospital, Ghafari St, Birjand University of Medical Sciences, Birjand, Iran, Phone: 985632626251, Email: [email protected]

Received Date: October 10, 2025

Published Date: October 28, 2025

Citation: Gholamhossein Y. (2025). Stargardt Disease a Clinical Finding of Circumb Papillary Band Shape Hyperpigmentery Hallow. Mathews J Ophthalmol. 10(1):38.

Copyrights: Gholamhossein Y. © (2025).

ABSTRACT

Introduction: The Stargardt disease is the most common cause of decreased of vision in adults of less than 50 years old. This disease is mutations in the ABCA4 gene which is located in the chromosome chain 1 short sleeve. It works by encode the ATP-binding cassette (ABC) protein transporter expressed by the outer trunk cell segment. Case Presentation: A 12 years old girl brought to eye clinic by parent due to visual complain, visual acuity with correction of the right eye and left eye was 20/200 and fundoscopic finding showed the macular lesion indeed of flecks retina finding. The circumb papillary band hyperpigmentery hallow finding may be a characteristic sub type feature of stargardet disease. Conclusion: A case of Stargardt disease has been reported in a 12-year-old girl. The circumb papillary band hyperpigmentery hallow may be a characteristic sub type feature of stargardet disease. Althought it needed to report othere cases and confrmatory paraclinical documentation.

Keywords: Stargardt’s Disease, Case Report, Circumb Papillary Band Hyperpigmentery Hallow.