{"id":13321,"date":"2024-08-23T01:34:01","date_gmt":"2024-08-22T23:34:01","guid":{"rendered":"https:\/\/valintermed.com\/?p=13321"},"modified":"2024-08-23T01:34:01","modified_gmt":"2024-08-22T23:34:01","slug":"vrozhdennaya-statsionarnaya-nochnaya-slepota-stseplennaya-s-h-hromosomoy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/congenital-static-nocturnal-blindness-stseplennaya-sh-hromosomoy\/","title":{"rendered":"X-linked congenital stationary night blindness"},"content":{"rendered":"
<\/div>\n

X-linked stationary night blindness (Oguchi disease) is a rare inherited disorder that affects males, while females can be carriers. This inherited disorder affects the light-sensitive cells of the retina responsible for perceiving light in low-light conditions. The main clinical manifestation of this disorder is the impairment of the ability to see in low light, thereby leading to night blindness. As the disease progresses, patients may experience changes in visual function up to the suppression of vision in daylight conditions, which is associated with the peculiarities of the functioning of the photoreceptors located in the light-sensitive area of the retina.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n