OGUCHI DISEASE – TWO PATIENTS WITH VARIABLE GENE MUTATION AND OPTICAL COHERENCE TOMOGRAPHY FINDINGS
Oguchi disease is a rare form of congenital stationary night blindness which has autosomal recessive inheritance. It is characterized by typical clinical features in which there is golden yellow tapetal reflex over the fundus which disappears after prolonged dark adaptation. This clinical character...
محفوظ في:
| المؤلفون الرئيسيون: | , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Army Medical College Rawalpindi
2016-12-01
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| سلاسل: | Pakistan Armed Forces Medical Journal |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://pafmj.org/PAFMJ/article/view/1288 |
| الوسوم: |
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