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Toplam kayıt 34, listelenen: 31-34
Multiple muscle hypoplasia in Poland's syndrome
(2008)
Poland's syndrome is a nonhereditary congenital disorder with unknown etiology, characterized by unilateral absence of pectoralis major muscle and various deformities of the ipsilateral upper extremity. The most common ...
Developing a computer program of laser aplication imaged with fundus fluorescein angiography test for retinal diseases
(Gazi Eye Foundation, 2016)
Purpose: The aim was to design a model which facilitates laser treatment for Diabetic Retinopathy and the treatment technique was conducted during education of assistant doctors. Materials and Methods: 127 patients diagnosed ...
Association between Stargardt's disease and Retinitis Pigmentosa: Is common genetic mutation responsible?
(2011)
In this study the association between Stargardt's disease (STGD) and Retinisitis Pigmentosa (RP), both of which is seen in a case with a mutated ABCA4 gene, is analysed. Fundus exaimination was performed to a 23 years old ...
An unilateral acute idiopathic maculopathy case: Masquerading as hereditary maculopathy
(Gazi Eye Foundation, 2014)
A 15-year-old male patient presented to our clinic with loss of central vision that began about 2 weeks before presentation. He diagnosed with hereditary maculopathy in another clinic. His visual acuity was 2/10. After he ...