{"id":13437,"date":"2024-08-22T23:35:23","date_gmt":"2024-08-22T21:35:23","guid":{"rendered":"https:\/\/valintermed.com\/?p=13437"},"modified":"2024-08-22T23:35:23","modified_gmt":"2024-08-22T21:35:23","slug":"h-stseplennaya-displaziya-setchatki","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/","title":{"rendered":"X-linked retinal dysplasia"},"content":{"rendered":"<div class=\"fpm_start\"><\/div>\n<p>X-linked retinal dysplasia (XLRD) is a rare inherited disorder characterized by abnormal development of the retina of the eye, which is inherited in an X-linked manner. This disorder results in various visual defects, including decreased visual acuity, and possible abnormalities in color perception. The disease most often affects males, as they have only one X chromosome, while females can be carriers without having any obvious symptoms. An important aspect of XLD is that the development of the disease can vary in severity, and clinical manifestations can vary from mild to severe.<\/p>\n<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_83 counter-flat ez-toc-counter ez-toc-light-blue ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title\" style=\"cursor:inherit\">Content<\/p>\n<span class=\"ez-toc-title-toggle\"><a href=\"#\" class=\"ez-toc-pull-right ez-toc-btn ez-toc-btn-xs ez-toc-btn-default ez-toc-toggle\" aria-label=\"Toggle Table of Content\"><span class=\"ez-toc-js-icon-con\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewbox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewbox=\"0 0 24 24\" version=\"1.2\" baseprofile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n<nav><ul class='ez-toc-list ez-toc-list-level-1 eztoc-toggle-hide-by-default' ><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%98%D1%81%D1%82%D0%BE%D1%80%D0%B8%D1%8F_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\" >History of the disease<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%AD%D0%BF%D0%B8%D0%B4%D0%B5%D0%BC%D0%B8%D0%BE%D0%BB%D0%BE%D0%B3%D0%B8%D1%8F\" >Epidemiology<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%93%D0%B5%D0%BD%D0%B5%D1%82%D0%B8%D1%87%D0%B5%D1%81%D0%BA%D0%B0%D1%8F_%D0%BF%D1%80%D0%B5%D0%B4%D1%80%D0%B0%D1%81%D0%BF%D0%BE%D0%BB%D0%BE%D0%B6%D0%B5%D0%BD%D0%BD%D0%BE%D1%81%D1%82%D1%8C\" >Genetic predisposition<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%A4%D0%B0%D0%BA%D1%82%D0%BE%D1%80%D1%8B_%D1%80%D0%B8%D1%81%D0%BA%D0%B0_%D0%B2%D0%BE%D0%B7%D0%BD%D0%B8%D0%BA%D0%BD%D0%BE%D0%B2%D0%B5%D0%BD%D0%B8%D1%8F\" >Risk factors for occurrence<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%94%D0%B8%D0%B0%D0%B3%D0%BD%D0%BE%D1%81%D1%82%D0%B8%D0%BA%D0%B0_%D0%B4%D0%B0%D0%BD%D0%BD%D0%BE%D0%B3%D0%BE_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\" >Diagnosis of this disease<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%9B%D0%B5%D1%87%D0%B5%D0%BD%D0%B8%D0%B5\" >Treatment<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%A1%D0%BF%D0%B8%D1%81%D0%BE%D0%BA_%D0%BB%D0%B5%D0%BA%D0%B0%D1%80%D1%81%D1%82%D0%B2_%D0%BF%D1%80%D0%B8%D0%BC%D0%B5%D0%BD%D1%8F%D0%B5%D0%BC%D1%8B%D1%85_%D0%B4%D0%BB%D1%8F_%D0%BB%D0%B5%D1%87%D0%B5%D0%BD%D0%B8%D1%8F\" >List of drugs used for treatment<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%9C%D0%BE%D0%BD%D0%B8%D1%82%D0%BE%D1%80%D0%B8%D0%BD%D0%B3_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\" >Disease monitoring<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%92%D0%BE%D0%B7%D1%80%D0%B0%D1%81%D1%82%D0%BD%D1%8B%D0%B5_%D0%BE%D1%81%D0%BE%D0%B1%D0%B5%D0%BD%D0%BD%D0%BE%D1%81%D1%82%D0%B8_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\" >Age-related features of the disease<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-10\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/h-stseplennaya-displaziya-setchatki\/#%D0%92%D0%BE%D0%BF%D1%80%D0%BE%D1%81%D1%8B_%D0%B8_%D0%BE%D1%82%D0%B2%D0%B5%D1%82%D1%8B\" >Questions and Answers<\/a><\/li><\/ul><\/nav><\/div>\n<h2><span class=\"ez-toc-section\" id=\"%D0%98%D1%81%D1%82%D0%BE%D1%80%D0%B8%D1%8F_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\"><\/span>History of the disease<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>The history of the study of X-linked retinal dysplasia goes back to the mid-20th century. The first descriptions of diseases involving retinal abnormalities were published in the 1960s, when doctors began to note inheritance patterns and clinical manifestations that could indicate a range of genetic disorders. Since then, key markers associated with these conditions have been identified. In the 1980s, scientists began to link specific mutations in genes encoding retinal proteins to disease manifestations. This area of research has evolved rapidly, and significant advances have been made in understanding the molecular basis of the disease.<\/p>\n<h2><span class=\"ez-toc-section\" id=\"%D0%AD%D0%BF%D0%B8%D0%B4%D0%B5%D0%BC%D0%B8%D0%BE%D0%BB%D0%BE%D0%B3%D0%B8%D1%8F\"><\/span>Epidemiology<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Epidemiological data indicate that X-linked retinal dysplasia is a rare disorder, occurring in approximately 1 in 30,000 male births. Due to the lack of reliable carrier statistics, it is often difficult to determine exact numbers in females, but it is expected that the number of carriers may be significantly higher. Overall, the prevalence of the disorder may also vary by geographic location and ethnic group. Specific mutations and their association with clinical manifestations also play an important role in determining the prevalence of the condition in different populations.<\/p>\n<h2><span class=\"ez-toc-section\" id=\"%D0%93%D0%B5%D0%BD%D0%B5%D1%82%D0%B8%D1%87%D0%B5%D1%81%D0%BA%D0%B0%D1%8F_%D0%BF%D1%80%D0%B5%D0%B4%D1%80%D0%B0%D1%81%D0%BF%D0%BE%D0%BB%D0%BE%D0%B6%D0%B5%D0%BD%D0%BD%D0%BE%D1%81%D1%82%D1%8C\"><\/span>Genetic predisposition<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>X-linked retinal dysplasia is caused by mutations in the RPGR (Retinitis Pigmentosa GTPase Regulator) gene, which is located on the X chromosome. Changes in this gene lead to dysfunction of the retina, which in turn causes degeneration of photoreceptors and other abnormalities. In addition to the RPGR gene, other genes such as RP2 and RPE65 have also been identified that may be involved in the pathogenesis of the disease. These genes are involved in cellular processes related to the maintenance and function of the retina, which again confirms the importance of genetic testing for diagnosis.<\/p>\n<h2><span class=\"ez-toc-section\" id=\"%D0%A4%D0%B0%D0%BA%D1%82%D0%BE%D1%80%D1%8B_%D1%80%D0%B8%D1%81%D0%BA%D0%B0_%D0%B2%D0%BE%D0%B7%D0%BD%D0%B8%D0%BA%D0%BD%D0%BE%D0%B2%D0%B5%D0%BD%D0%B8%D1%8F\"><\/span>Risk factors for occurrence<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Risk factors for X-linked retinal dysplasia include heredity, as the condition is passed down through families. It is also important to consider possible environmental factors, such as exposure to certain toxic substances and radiation, especially during fetal development. However, specific physical or chemical factors that directly increase the risk of developing the condition have not been identified. Research highlights the importance of genetic predispositions, as well as the influence on the behavior of carriers, who may develop symptoms later in life.<\/p>\n<h2><span class=\"ez-toc-section\" id=\"%D0%94%D0%B8%D0%B0%D0%B3%D0%BD%D0%BE%D1%81%D1%82%D0%B8%D0%BA%D0%B0_%D0%B4%D0%B0%D0%BD%D0%BD%D0%BE%D0%B3%D0%BE_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\"><\/span>Diagnosis of this disease<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Diagnosis of X-linked retinal dysplasia involves several important steps:<\/p>\n<ul>\n<li>Main symptoms: decreased visual acuity, low-brightness conditions, problems with color perception.<\/li>\n<li>Laboratory tests: Genetic testing to identify mutations in relevant genes.<\/li>\n<li>Radiological examinations: use of optical coercion tomography (OCT) and fluorescein angiography to assess the condition of the retina.<\/li>\n<li>Other types of diagnostics: systematic monitoring of the development of clinical symptoms.<\/li>\n<\/ul>\n<p>The differential diagnosis includes other pertinent conditions such as retinitis pigmentosa and other hereditary retinal disorders.<\/p>\n<h2><span class=\"ez-toc-section\" id=\"%D0%9B%D0%B5%D1%87%D0%B5%D0%BD%D0%B8%D0%B5\"><\/span>Treatment<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Treatment for X-linked retinal dysplasia currently focuses on managing symptoms and slowing disease progression. <\/p>\n<ul>\n<li>General treatment: providing patients with the necessary visual devices and adapting the environment.<\/li>\n<li>Pharmacological treatment: There are currently no specific medications, but various antioxidants may help support retinal health.<\/li>\n<li>Surgical treatment: In particularly severe cases, surgical intervention options may be considered.<\/li>\n<li>Other treatments: Gene therapy and cell therapy are also being explored to restore retinal function at the molecular level.<\/li>\n<\/ul>\n<h2><span class=\"ez-toc-section\" id=\"%D0%A1%D0%BF%D0%B8%D1%81%D0%BE%D0%BA_%D0%BB%D0%B5%D0%BA%D0%B0%D1%80%D1%81%D1%82%D0%B2_%D0%BF%D1%80%D0%B8%D0%BC%D0%B5%D0%BD%D1%8F%D0%B5%D0%BC%D1%8B%D1%85_%D0%B4%D0%BB%D1%8F_%D0%BB%D0%B5%D1%87%D0%B5%D0%BD%D0%B8%D1%8F\"><\/span>List of drugs used for treatment<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>At present, the list of drugs used for maintenance therapy of X-linked retinal dysplasia remains limited and may include:<\/p><script data-noptimize=\"\" data-wpfc-render=\"false\">\nfpm_start( \"true\" );\n<\/script>\n\n<ul>\n<li>Vitamin complexes with antioxidants such as vitamin A, C and E;<\/li>\n<li>Systemic drugs that support visual functions;<\/li>\n<li>Local drugs used to treat concomitant eye diseases.<\/li>\n<\/ul>\n<h2><span class=\"ez-toc-section\" id=\"%D0%9C%D0%BE%D0%BD%D0%B8%D1%82%D0%BE%D1%80%D0%B8%D0%BD%D0%B3_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\"><\/span>Disease monitoring<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Monitoring of a patient with X-linked retinal dysplasia includes regular ophthalmologic examinations to assess disease progression and adjust treatment options. The prognosis varies depending on the severity of the disease, but most patients are at risk of developing serious complications associated with vision loss. Therefore, early diagnosis and regular monitoring are important.<\/p>\n<h2><span class=\"ez-toc-section\" id=\"%D0%92%D0%BE%D0%B7%D1%80%D0%B0%D1%81%D1%82%D0%BD%D1%8B%D0%B5_%D0%BE%D1%81%D0%BE%D0%B1%D0%B5%D0%BD%D0%BD%D0%BE%D1%81%D1%82%D0%B8_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8F\"><\/span>Age-related features of the disease<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>X-linked retinal dysplasia may manifest itself at different ages. In newborns and younger children, manifestations may be hidden, which requires careful monitoring by pediatricians and ophthalmologists. In adolescence, symptoms often become more pronounced, which requires the beginning of active therapy and conditions for adapting patients&#039; lives to their limited visual functions.<\/p>\n<h2><span class=\"ez-toc-section\" id=\"%D0%92%D0%BE%D0%BF%D1%80%D0%BE%D1%81%D1%8B_%D0%B8_%D0%BE%D1%82%D0%B2%D0%B5%D1%82%D1%8B\"><\/span>Questions and Answers<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<ul>\n<li><strong>Who is at risk for developing X-linked retinal dysplasia?<\/strong> Males who pass on genetic mutations to their future offspring; female carriers who may not show symptoms.<\/li>\n<li><strong>What are the main symptoms of this disease?<\/strong> Decreased visual acuity, difficulty perceiving colors, poor visibility in low-brightness conditions.<\/li>\n<li><strong>How is X-linked retinal dysplasia diagnosed?<\/strong> Diagnosis involves symptomatic testing, laboratory genetic tests, and radiological examination methods.<\/li>\n<li><strong>Are there specific treatments for X-linked retinal dysplasia?<\/strong> There is currently no specific treatment, but supportive care may reduce symptoms.<\/li>\n<li><strong>What is the degree of progression of the disease?<\/strong> Progression can vary, and most patients experience long-term complications, including complete vision loss.<\/li>\n<\/ul>\n<div class=\"fpm_end\"><\/div>","protected":false},"excerpt":{"rendered":"<p>X-linked retinal dysplasia (XLRD) is a rare inherited disorder characterized by abnormal development of the retina of the eye, which is inherited in an X-linked manner. It<\/p>","protected":false},"author":1,"featured_media":24252,"comment_status":"open","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[298],"tags":[],"class_list":["post-13437","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-medlibrary"],"_links":{"self":[{"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/posts\/13437","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/comments?post=13437"}],"version-history":[{"count":1,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/posts\/13437\/revisions"}],"predecessor-version":[{"id":13480,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/posts\/13437\/revisions\/13480"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/media\/24252"}],"wp:attachment":[{"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/media?parent=13437"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/categories?post=13437"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/tags?post=13437"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}