- retinal dystrophy
- дистрофия сетчатки
English-Russian dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков. 2015.
retinal dystrophy
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Dystrophy — is any condition of abnormal development, often denoting the degeneration of muscles. Types Muscular dystrophy Duchenne muscular dystrophy Becker s muscular dystrophy Reflex neurovascular dystrophy Retinal dystrophy Conal dystrophy Myotonic… … Wikipedia
dystrophy — Progressive changes that may result from defective nutrition of a tissue or organ. SYN: dystrophia. [dys + G. trophe, nourishment] adiposogenital d. a disorder characterized primarily by obesity and hypogonadotrophic hypogonadism … Medical dictionary
Cone dystrophy — Classification and external resources Fundus of a 34 year old patient with cone rod dystrophy due to Spinocerebellar Ataxia Type 7 (SCA7). Note that the macular area, and also the mid periphery, are atrophic … Wikipedia
Doyne honeycomb dystrophy — Doyne honeycomb retinal dystrophy an autosomal dominant degenerative eye condition marked by light colored patches near the optic disk and macula; called also Doyne colloid degeneration and Doyne honeycomb choroiditis or degeneration … Medical dictionary
Corneal dystrophy (human) — Main article: corneal dystrophy Corneal dystrophy (human) Classification and external resources ICD 10 H18.5 ICD 9 … Wikipedia
Fuchs' dystrophy — Classification and external resources Fuchs corneal dystrophy. Light microscopic appearance of the cornea showing numerous excrescences (guttae) on the posterior surface of Descemet s membrane and the presence of cysts in the corneal epithelium… … Wikipedia
Meesmann juvenile epithelial corneal dystrophy — Classification and external resources Multiple opaque spots in the corneal epithelium ICD … Wikipedia
Progressive retinal atrophy — (PRA) is a group of genetic diseases seen in certain breeds of dogs and, more rarely, cats. It is characterized by the bilateral degeneration of the retina, causing progressive vision loss culminating in blindness. The condition in nearly all… … Wikipedia
Facioscapulohumeral muscular dystrophy — FSHD redirects here. For other uses, see FSHD (disambiguation). Facioscapulohumeral muscular dystrophy Classification and external resources ICD 10 G71.0 ICD 9 … Wikipedia
RPE65 — Retinal pigment epithelium specific protein 65kDa, also known as RPE65, is a human gene.cite web | title = Entrez Gene: RPE65 retinal pigment epithelium specific protein 65kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
