Coats’ Disease: Pathogenesis, Diagnosis, and Treatment
نویسندگان
چکیده
Coats disease is an idiopathic nonhereditary condition retinal vascular disorder characterized by telangiectasia with intraretinal and/ or subretinal exudation. Unilateral involvement in young males the typical presentation most cases being diagnosed first and second decade of life and, if untreated, can lead to total detachment secondary glaucoma, sometimes requiring enucleation. The common presenting complaints include decreased vision, strabismus, leukocoria. This article describes clinical features, pathophysiology, classification staging, complications, differential diagnosis, management disease.
منابع مشابه
Frozen shoulder: Pathogenesis, Diagnosis and Treatment
Frozen shoulder (FS) or adhesive capsulitis is a common disease which causes pain, difficulty and restriction in the movement of the shoulder joint due to unclear complex etiology. The everyday tasks such as bathing, dressing and driving become difficult. It affects both men and women especially in their 40s and 60s. The duration of the disease varies from one patient to another and it may last...
متن کاملFerroportin disease: pathogenesis, diagnosis and treatment
Ferroportin Disease (FD) is an autosomal dominant hereditary iron loading disorder associated with heterozygote mutations of the ferroportin-1 (FPN) gene. It represents one of the commonest causes of genetic hyperferritinemia, regardless of ethnicity. FPN1 transfers iron from the intestine, macrophages and placenta into the bloodstream. In FD, loss-of-function mutations of FPN1 limit but do not...
متن کاملFabry's disease--a comprehensive review on pathogenesis, diagnosis and treatment.
Fabry's is a progressive, destructive and life threatening disease which reduces significantly life expectancy of the affected individual. It is a genetic disorder of X-linked inheritance caused by deficiency of lysosomal enzyme alpha-galactosidase A resulting in progressive accumulation of glycosphingolipids within different body cells. Fabry's deposits are defined histopathologically as lamel...
متن کاملImmunoglobulin G4-related kidney disease: Pathogenesis, diagnosis, and treatment
Immunoglobulin G4-related disease (IgG4-RD) is a recently recognized clinical entity that often involves multiple organs; it is characterized by high levels of serum immunoglobulin G4 (IgG4), dense infiltration of IgG4+ cells, and storiform fibrosis. Cellular immunity, particularly T cell-mediated immunity, has been implicated in the pathogenesis of IgG4-RD. The most frequent renal manifestatio...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Güncel retina
سال: 2023
ISSN: ['2564-7156', '2548-0693']
DOI: https://doi.org/10.37783/crj-0357