Congenital ectropion uveae
MONDO:0019630Congenital ectropion uveae is a rare, genetic, non-syndromic developmental defect of the eye characterized by the presence of iris pigment epithelium on the anterior surface of the iris, anterior insertion of the iris, angle dysgenesis and progressive open-angle glaucoma (the latter may present in infancy or may develop later in life). Patients may manifest with headaches, ocular pain, photophobia, and redness, watering and/or swelling of the eye. It can often be associated with neurofibromatosis and less commonly with other ocular abnormalities.
10 clinical trials for this condition and its sub-types.
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Disease
(618)
Hereditary disease
(172)
Eye disorder
(97)
Human disease
(14)
Disorder of orbital region
(3)
Anterior segment dysgenesis
(2)
Disease of genetic or genomic mechanism
(2)
Disorder of visual system
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)