Fuchs' heterochromic cyclitis and retinal vascular abnormalities in progressive hemifacial atrophy
نویسندگان
چکیده
منابع مشابه
Glaucoma in Fuchs' heterochromic cyclitis associated with congenital Horner's syndrome.
We report a retrospective study of five patients with monocular Fuchs' heterochromic cyclitis associated with an ipsilateral Horner's syndrome. The minimum follow-up was 10 years. The presenting findings were cyclitis in three of the patients and heterochromia iridis associated with blepharoptosis in the other two. The major factors affecting all five patients were cataract and glaucoma. The in...
متن کاملContralateral active ocular toxoplasmosis in Fuchs' heterochromic cyclitis.
1 Jampol LM, Sieving PA, Pugh D, Fishman GA, Gilbert H. Multiple evanescent white dot syndrome: I. Clinical findings. Arch Ophthalmol 1984; 102: 671-4. 2 Sieving PA, Fishman GA, Jampol LM, Pugh D. Multiple evanescent white dot syndrome: II. Electrophysiology of the photoreceptors during retinal pigment epithelial disease. Arch Ophthalmol 1984; 102: 675-9. 3 Dodwell DG, Jampol LM, Rosenberg M, B...
متن کاملImmunity to a corneal antigen in Fuchs' heterochromic cyclitis patients.
Immunity to a major corneal antigen was studied in 28 Fuchs' heterochromic cyclitis patients and compared with the response of 44 patients with other types of uveitis and 19 healthy controls. The highest incidence of immune response was found in patients with anterior segment involvement only (anterior uveitis and Fuchs') whereas the frequency of anti-corneal immune response in patients with po...
متن کامل[Fuchs' heterochromic cyclitis without heterochromia: a diagnostic approach].
OBJECTIVE To obtain diagnostic guidelines of Fuchs' heterochromic cyclitis (FHC) in the absence of heterochromia using Bayesian methods. METHODS The pre-test and post-test likelihood that a certain patient without heterochromia (but with other characteristic symptoms of the disease such as iris nodules, cataracts, glaucoma or vitritis) has FCH, was assessed by the Bayes' theorem for condition...
متن کاملProgressive hemifacial atrophy
Progressive hemifacial atrophy, also known as Parry-Romberg Syndrome, is an uncommon degenerative and poorly understood condition. It is characterized by a slow and progressive but self-limited atrophy affecting one side of the face. The incidence and the cause of this alteration are unknown. A cerebral disturbance of fat metabolism has been proposed as a primary cause. Possible factors that ar...
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ژورنال
عنوان ژورنال: Eye
سال: 1993
ISSN: 0950-222X,1476-5454
DOI: 10.1038/eye.1993.84