Foveal Hypoplasia in Oculocutaneous Albinism and the Role of OCT

Autor:	Paul R, Shanmugalingam S, Kulshrestha M, Barr D
Rok vydání:	2015
Předmět:	Refractive error Coloboma medicine.medical_specialty genetic structures Photophobia business.industry Usher syndrome medicine.disease Oculocutaneous albinism eye diseases Hypoplasia Foveal Ophthalmology Materials Chemistry medicine Albinism Optometry sense organs medicine.symptom business
Zdroj:	Advances in Ophthalmology & Visual System. 2
ISSN:	2377-4290
DOI:	10.15406/aovs.2015.02.00045
Popis:	We describe a case of a 16 year old girl with Oculocutaneous albinism (OCA) who presented to us with photophobia and blurring of vision. She showed typical features of OCA, blonde hair, refractive error, iris transillumination and foveal hypoplasia. Our report highlights the role of macular OCT in diagnosis of foveal hypoplasia which is an essential feature of OCA.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::431e283690007218a7c4b7e2ddc062c7 https://doi.org/10.15406/aovs.2015.02.00045 Zobrazit plný text záznamu