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Renal dysplasia-retinal aplasia syndrome. Senior–Løken syndrome is an autosomal recessive inherited condition. Specialty. Medical genetics. Senior–Løken syndrome is a congenital eye disorder, first characterized in 1961. [1] [2] [3] It is a rare, ciliopathic, autosomal recessive disorder characterized by juvenile nephronophthis and ...
Oculogyric crisis ( OGC) is a rare sudden, paroxysmal, dystonic reaction that may manifest in response to specific drugs, particularly neuroleptics, or medical conditions, such as movement disorders. This neurological phenomenon is characterized by a sustained dystonic, conjugate, involuntary upward deviation of both eyes lasting seconds to hours.
To measure treatment outcome the sum of the ten items is used. A higher score signifies deeper depression. When using the scale to diagnose depression according to ICD-10, there are the following possibilities: Mild depression: A score of 4 or 5 in two of the first three items. Plus a score of at least 3 on two or three of the last seven items.
Ocular myasthenia gravis (MG) is a disease of the neuromuscular junction resulting in hallmark variability in muscle weakness and fatigability. MG is an autoimmune disease where anomalous antibodies are produced against the naturally occurring acetylcholine receptors in voluntary muscles. MG may be limited to the muscles of the eye (ocular MG ...
H15-H22 Disorders of sclera, cornea, iris and ciliary body. (H15.0) Scleritis — a painful inflammation of the sclera. (H16) Keratitis — inflammation of the cornea. (H16.0) Corneal ulcer / Corneal abrasion — loss of the surface epithelial layer of the eye's cornea. (H16.1) Snow blindness / Arc eye — a painful condition caused by exposure ...
This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes H00-H59 within Chapter VII: Diseases of the eye, adnexa should be included in this category.
Pseudoexfoliation syndrome, often abbreviated as PEX [1] and sometimes as PES or PXS, is an aging-related systemic disease manifesting itself primarily in the eyes which is characterized by the accumulation of microscopic granular amyloid-like protein fibers. [2] Its cause is unknown, although there is speculation that there may be a genetic basis.
Visual snow syndrome. Visual Snow can appear at any time, but it commonly appears at birth, late teenage years, and early adulthood. Visual snow syndrome ( VSS) is an uncommon neurological condition in which the primary symptom is that affected individuals see persistent flickering white, black, transparent, or colored dots across the whole ...