A significant reduction in CCT was observed at the 6th, 12th, and 24th months with latanoprost and bimatoprost. Serial CCT measurements in determining the IOP values may be helpful in the follow-up of prostaglandin analogs.

Objectives:To evaluate the clinical and demographic properties of Fuchs’ uveitis syndrome (FUS) in Turkish patients.Materials and Methods:The medical records of 161 patients with FUS followed in the Uveitis Division of Ulucanlar Eye Hospital between 1996 and 2014 were respectively reviewed. The mean age at diagnosis, sex, the number of affected eyes, follow-up period, clinical findings at presentation, complications during the follow-up period, medical and surgical treatments, and best corrected visual acuity at the initial and final visits were recorded.Results:The study included 171 eyes of 161 patients diagnosed with FUS. Of the patients, 94 (58.4%) were female and 67 (41.6%) were male. The mean age at presentation was 35.2±11.0 (11-65) years. The mean follow-up period was 23.5±32.8 (2-216) months. Ten (6.2%) patients had bilateral involvement. The most common symptoms at presentation were decreased visual acuity or blurred vision in 63 (39.1%) and floaters in 19 (11.8%) patients. Clinical findings at presentation included diffuse small, round, white keratic precipitates in 128 (74.8%) eyes, anterior chamber reaction in 82 (47.9%), vitreous cells in 122 (71.3%), heterochromia in 47 (27.4%) and iris nodules in 32 (18.7%) eyes. During the follow-up period, elevated intraocular pressure occured in 31 (18.1%) eyes and the most common complication was cataract development (89 eyes, 52.0%).Conclusion:Heterochromia was observed in 27.4% of patients in our study. However, the diffuse small, round keratic precipitates, low-grade anterior chamber reaction and varying degrees of vitreous reaction are more common clinical characteristics that are helpful in making the diagnosis.

Childhood migraine does not cause changes in posterior ocular structure parameters.

Ö ÖZ ZE ET T A Am ma aç ç: : Oküler motor kraniyal sinir paralizisi olan hastaların etiyolojik ve klinik seyrinin retrospektif olarak değerlendirilmesidir. G Ge er re eç ç v ve e Y Yö ön nt te em ml le er r: : Çalışmamıza, Ulucanlar Göz Eğitim ve Araştırma Hastanesi Nörooftalmoloji Bölümüne 2003-2013 yılları arasında ardışık başvuran, düzenli takipleri olan 98 hasta dâhil edildi. Tüm hastaların ayrıntılı tıbbi öyküleri alındı, nörooftalmolojik muayeneleri yapıldı. Hastaların yaşı, cinsiyeti, eşlik eden sistemik hastalıkları, etiyolojisi, pupil çapı, pitozis varlığı ve şiddeti ve Hess ekranı ile değerlendirilen göz hareketleri geriye dönük olarak değerlendirildi. Etiyolojiye yönelik olarak görüntüleme yöntemlerine başvuruldu. B Bu ul lg gu ul la ar r: : Hastaların 45 (%45,9)'i kadın, 53 (%54,1)'ü erkek idi. Başvuru anındaki yaş ortalaması 53,6±17,5 (7-90) yıl idi. Ortalama izlem süresi 6,6±8,1 (3-64) ay idi. Her iki göz tutulumu 5 (%5,1) hastada mevcuttu. En sık izole altıncı kraniyal sinir (%48,9) felci izlenirken, bunu izole üçüncü kraniyal sinir (%34,6) felci izledi. İzole troklear sinir felci ise %15,3 oranında saptandı. Birden çok oküler motor sinir tutulumu ise 2 (%2,0) hastada izlendi. Oküler motor sinir felci ile pitoz %76,4 ve anizokori %17,6 oranında birliktelik göstermekte idi. Etiyolojik dağılımda hem altıncı sinir hem üçüncü kraniyal sinir için vaskü-ler sebepler (sırasıyla %68,7; %63,8), dördüncü kraniyal sinir felcinde ise kafa travması (%37,5) ön planda idi. S So on nu uç ç: : Bizim serimizde, oküler motor kraniyal sinir paralizilerinden en sık altıncı kraniyal sinir felci saptanırken, vasküler sebepler etiyolojik dağılımda ön planda idi. Imaging methods were used as required to determine the etiology. R Re es su ul lt ts s: : There were 45 (45.9%) female and 53 (54.1%) male patients. The mean age at presentation was 53.6±17.5 (7-90) years. The mean follow-up period was 6.6±8.1 (3-64) months. Five (5.1%) cases had bilateral involvement. The most commonly affected nerve was the sixth cranial nerve (48.9%) followed by the third cranial nerve (34.6%). Trochlear nerve palsy was identified at a rate of 15.3%. Multiple ocular nerve palsies were observed in 2 (2.0%) cases. Accompanying ptosis was found in 76.4% and anisocoria in 17.6%. The main cause was vascular disorders for both sixth and third cranial nerve palsy (68.7% and 63.8%, respectively) and head trauma for fourth cranial nerve palsy (37.5%). C Co on nc cl lu us si io on n: : Sixth cranial nerve palsy was the most common ocular motor cranial nerve palsy and a vascular disorder was the most frequent cause of these disorders.

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