Ads
related to: treatment for retinal dystrophy disease
Search results
Results from the WOW.Com Content Network
The Argus retinal prosthesis became the first approved treatment for the disease in February 2011, and is currently available in Germany, France, Italy, and the UK. [39] Interim results on 30 patients long term trials were published in 2012. [40] The Argus II retinal implant has also received market approval in the US. [41]
Vitelliform macular dystrophy is an irregular autosomal dominant eye disorder which can cause progressive vision loss. [1] This disorder affects the retina , specifically cells in a small area near the center of the retina called the macula .
Sorsby's fundus dystrophy is an autosomal dominant, retinal disease characterized by sudden acuity loss resulting from untreatable submacular neovascularisation Stargardt's disease (juvenile macular degeneration, STGD) is an autosomal recessive retinal disorder characterized by juvenile-onset macular dystrophy, alterations of the peripheral ...
The analyst views the appeal of gene therapies in retinal disease overall as decreasing, thus reducing the assumed share of patients who are likely to opt for these treatments.
Occult macular dystrophy (OMD) is a rare inherited degradation of the retina, characterized by progressive loss of function in the most sensitive part of the central retina , the location of the highest concentration of light-sensitive cells (photoreceptors) but presenting no visible abnormality.
Cone dystrophy; Fundus of a 45 year-old patient with cone rod dystrophy segregating with a loss-of-function mutation (E1087X) in ABCA4. Note the presence of various-shaped pigment deposits in the posterior pole with atrophy of the retina, while the retina appears less damaged in periphery (upper part of the photograph).
Stargardt disease is the most common inherited single-gene retinal disease. [1] In terms of the first description of the disease, [ 2 ] it follows an autosomal recessive inheritance pattern, which has been later linked to bi-allelic ABCA4 gene variants (STGD1).
ROSAH stands for retinal dystrophy, optic nerve edema, splenomegaly, anhidrosis and headache. The name emphasizes some, but not all, of the features that can be associated with the syndrome. [ 2 ] The disease is inherited in an autosomal dominant manner and caused by heterozygous missense mutations in the ALPK1 gene , an innate immune sensor ...
Ads
related to: treatment for retinal dystrophy disease