Case series of Stargardt's disease: Our experience

Authors

  • Syed Abdul Wadud Department of Community Ophthalmology, Bangabandhu Sheikh Mujib Medical University, Kazi Nazrul Islam Avenue, Shahbag, Dhaka
  • Muntasir Bin Shahid Department of Community Ophthalmology, Bangabandhu Sheikh Mujib Medical University, Kazi Nazrul Islam Avenue, Shahbag, Dhaka
  • Sumon Afroz Department of Community Ophthalmology, Bangabandhu Sheikh Mujib Medical University, Kazi Nazrul Islam Avenue, Shahbag, Dhaka

DOI:

https://doi.org/10.3329/bsmmuj.v7i2.29452

Keywords:

Central visual field loss, Optical coherence tomography, Stargardt's disease

Abstract

Stargardt disease is the most common form of juvenile macular degeneration. Clinically, it is characterized by pisciform flecks at lhe level of the retinal pigment epithelium and a bull's-eye maculopathy. Inheritance is usually autosomal recessive, although dominantly inherited case have been described. Both sexes are affected equally. We reported here three cases of Stargardt's macular dystrophy, who are siblings and daughters of non consanguineous parents. In case-1,2 and 3 we found the typical presentation with almost same findings.

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Published

2016-08-24

How to Cite

Wadud, S. A., Shahid, M. B., & Afroz, S. (2016). Case series of Stargardt’s disease: Our experience. Bangabandhu Sheikh Mujib Medical University Journal, 7(2), 147–150. https://doi.org/10.3329/bsmmuj.v7i2.29452

Issue

Section

Case Reports