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The state of the organ of vision in hereditary kidney pathology in children

Poster Details

First Author: N.Karimjanova UZBEKISTAN

Co Author(s):    D. Makhkamova                    

Abstract Details

Purpose:

To study the state of the organ of vision in hereditary kidney pathology in children.

Setting:

Tashkent Institute of Postgraduate Medical Education.

Methods:

17 patients aged 5 to 14 years with verified hereditary diseases of the kidneys were examined: hereditary nephritis 5 (31%), polycystic kidney 7 (25%), renal diabetes insipidus 4 (28%). Ophthalmic examinations included visometry, biomicroscopy, perimetry, tonography and ophthalmoscopy.

Results:

In children with hereditary kidney diseases, various changes in the eye have been identified: refractive errors of u15 (75%), congenital changes in the iris in the form of a residual pupillary membrane - 10 (50%), changes in the lens in the form of single point opacities and seals around the joints -13 (65%), changes in the vitreous body - 9 (45%), heterophory -3 (15%).

Conclusions:

On the basis of the data obtained, it can be concluded that children with hereditary diseases of the kidneys need to conduct an ophthalmological examination in order to early detection and treatment of their possible pathology of the organ of vision.

Financial Disclosure:

None

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