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Toxic anterior segment syndrome is an acute, sterile anterior segment inflammation following generally uneventful cataract and anterior segment surgery. [ 1 ] One of the main factors in differentiating toxic anterior segment syndrome from an infectious endophthalmitis is the rapid onset.
Ataxia telangiectasia (Louis–Bar syndrome) Encephalotrigeminal angiomatosis (Sturge–Weber syndrome) (encephalofacial cavernous hemangiomatosis) Neurofibromatosis (von Recklinghausen's disease) Tuberous sclerosis (Bourneville's syndrome) Wyburn–Mason syndrome (racemose hemangiomatosis)
Axenfeld–Rieger syndrome is a rare autosomal dominant [2] disorder, which affects the development of the teeth, eyes, and abdominal region. [3]Axenfeld–Rieger syndrome is part of the so-called iridocorneal or anterior segment dysgenesis syndromes, [4] which were formerly known as anterior segment cleavage syndromes, anterior chamber segmentation syndromes or mesodermal dysgenesis.
Acute idiopathic blind spot enlargement syndrome (AIBSE) is a rare eye disease affecting the retina of the eye. It is basically a type of retinopathy which affects females more than males. Currently there is no treatment for this condition, but, it is usually self limiting.
Symptoms may disappear if untreated, but treatment may decrease both the healing time and the chances of remission. [citation needed] Artificial tear eye-drops or ointments may be a suitable treatment for mild cases. Low-dosage steroidal eye-drops, such as prednisone, fluorometholone, loteprednol (Lotemax 0.5%) or rimexolone.
A toddler was diagnosed with retinal cancer and had to have her eye removed after the only symptom the little girl experienced was swelling around her eye.. Arkansas father Josh Morss said he ...
The varied signs and symptoms of Duane-radial ray syndrome often overlap with features of other disorders. For example, acro-renal-ocular syndrome is characterized by Duane anomaly and other eye abnormalities, radial ray malformations, and kidney defects. Both conditions can be caused by mutations in the same gene. [5]
However, it may definitely be related to other diseases included in the white dot syndrome group. Acute zonal occult outer retinopathy occurs in young to middle age adults and may eventually progress to retinal cell death. Symptoms include acute visual field loss and photopsias. Suspected causes include autoimmune, viral, and fungal. [2] [5]