scholarly journals Phacoemulsification in bilateral anterior lenticonus in Alport syndrome

Medicine ◽  
2019 ◽  
Vol 98 (39) ◽  
pp. e17054 ◽  
Author(s):  
Mohammad-Reza Sedaghat ◽  
Hamed Momeni-Moghaddam ◽  
Batool Haghighi ◽  
Majid Moshirfar
2007 ◽  
Vol 33 (6) ◽  
pp. 1127-1130 ◽  
Author(s):  
Mohammad Ali Zare ◽  
Mohammad Taher Rajabi ◽  
Mehdi Nili-Ahmadabadi ◽  
Syed Jafar Oskouee ◽  
Sasan Moghimi

2008 ◽  
Vol 36 (6) ◽  
pp. 1440-1444 ◽  
Author(s):  
YB Liu ◽  
SJ Tan ◽  
ZY Sun ◽  
X Li ◽  
BY Huang ◽  
...  

The case of a 29-year-old man is reported who presented with a gradually progressive, painless decrease in vision over 10 years. Anterior segment examination with a slit lamp revealed anterior lenticonus in both eyes. The patient had previously been diagnosed with bilateral sensorineural deafness, however investigations revealed microscopic haematuria and renal insufficiency that subsequently led to a diagnosis of classical Alport syndrome. Since the patient's quality of vision was severely affected by the bulging anterior lens capsule, surgical treatment was required. Clear lens phacoemulsification with continuous curvilinear capsulorhexis and foldable intraocular lens implantation were performed in each eye 2 days apart. One week after surgery, visual acuity was excellent in both eyes. Clear lens phacoemulsification with continuous curvilinear capsulorhexis and foldable intraocular lens implantation was a safe and effective therapeutic choice in this patient for the management of anterior lenticonus due to Alport syndrome.


2015 ◽  
Vol 25 (6) ◽  
pp. 507-511 ◽  
Author(s):  
Monika Ecsedy ◽  
Gúbor L. Súndor ◽  
Úgnes I. Takúcs ◽  
Kinga Krúnitz ◽  
Zoltún Kiss ◽  
...  

2020 ◽  
Vol 11 (1) ◽  
pp. 79-84
Author(s):  
Kathrine O. Eriksen ◽  
Øystein Kalsnes Jørstad

Alport syndrome is associated with various ocular phenotypic features, including several retinal manifestations. The purpose of this case report was to describe a case of multiple vitelliform lesions in Alport syndrome. This particular finding has, to our knowledge, not been reported previously. A 63-year-old man with known Alport syndrome presented with symptomatic, bilateral anterior lenticonus. Fundoscopic examination revealed multiple vitelliform lesions, which were symmetrically distributed at the posterior poles. Additional retinal findings included an irregular foveal contour and central macular thinning in both eyes, as well as a multilayered retinoschisis in the left eye. The underlying pathophysiology of the vitelliform lesions may be a dysfunctional Bruch’s membrane.


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