DOAJ Open Access 2016

Case series of Stargardt's disease: Our experience

Syed Abdul Wadud Muntasir Bin Shahid Sumon Afroz

Abstrak

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.

Topik & Kata Kunci

Medicine

Penulis (3)

Syed Abdul Wadud

Muntasir Bin Shahid

Sumon Afroz

Format Sitasi

APA MLA BibTeX

Wadud, S.A., Shahid, M.B., Afroz, S. (2016). Case series of Stargardt's disease: Our experience. https://doi.org/10.3329/bsmmuj.v7i2.29452

Akses Cepat

PDF tidak tersedia langsung

Cek di sumber asli →

Lihat di Sumber doi.org/10.3329/bsmmuj.v7i2.29452

Informasi Jurnal

Tahun Terbit: 2016
Sumber Database: DOAJ
DOI: 10.3329/bsmmuj.v7i2.29452
Akses: Open Access ✓