{"id":13063,"date":"2024-08-23T05:51:09","date_gmt":"2024-08-23T03:51:09","guid":{"rendered":"https:\/\/valintermed.com\/?p=13063"},"modified":"2024-08-23T05:51:09","modified_gmt":"2024-08-23T03:51:09","slug":"spinotserebellyarnaya-ataksiya-tip-2","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-injury-tip-2\/","title":{"rendered":"Spinocerebellar ataxia type 2"},"content":{"rendered":"<div class=\"fpm_start\"><\/div>\n<p>Spinocerebellar ataxia type 2 (SCA2) is an inherited neurodegenerative disorder characterized by progressive ataxia, motor incoordination, and other neurological symptoms such as dysarthria and decreased muscle tone. The disease is associated with dysfunction of the cerebellum and spinal cord, resulting in impaired motor control and balance. The underlying cause of CCA2 is abnormal expansions of CAG repeats in the ATXN2 gene, leading to accumulation of abnormal protein and neuronal damage. Evaluation of patients with this disorder requires a multidisciplinary approach, including neurological, genetic, and therapeutic aspects, to provide quality care and support.<\/p>\n<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_85 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\/spinal-cord-injury-tip-2\/#%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_%D0%B8_%D0%B8%D0%BD%D1%82%D0%B5%D1%80%D0%B5%D1%81%D0%BD%D1%8B%D0%B5_%D0%B8%D1%81%D1%82%D0%BE%D1%80%D0%B8%D1%87%D0%B5%D1%81%D0%BA%D0%B8%D0%B5_%D1%84%D0%B0%D0%BA%D1%82%D1%8B\" >History of the disease and interesting historical facts<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-injury-tip-2\/#%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\/spinal-cord-injury-tip-2\/#%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_%D0%BA_%D0%B4%D0%B0%D0%BD%D0%BD%D0%BE%D0%BC%D1%83_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8E\" >Genetic predisposition to this disease<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-injury-tip-2\/#%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_%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\" >Risk factors for the development of this disease<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-injury-tip-2\/#%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\/spinal-cord-injury-tip-2\/#%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\/spinal-cord-injury-tip-2\/#%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_%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\" >List of medications used to treat this disease<\/a><\/li><li class='ez-toc-page-1'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-injury-tip-2\/#%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\/spinal-cord-injury-tip-2\/#%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\/spinal-cord-injury-tip-2\/#%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_%D0%B8_%D0%B8%D0%BD%D1%82%D0%B5%D1%80%D0%B5%D1%81%D0%BD%D1%8B%D0%B5_%D0%B8%D1%81%D1%82%D0%BE%D1%80%D0%B8%D1%87%D0%B5%D1%81%D0%BA%D0%B8%D0%B5_%D1%84%D0%B0%D0%BA%D1%82%D1%8B\"><\/span>History of the disease and interesting historical facts<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Spinocerebellar ataxia was first described in the early 20th century as a disorder caused by genetic mutations. CCA2 was detailed by scientists as a distinct phenotype in 1993, when molecular genetics showed that the disorder was associated with an expansion of CAG repeats in the ATXN2 gene. The discovery of this gene initiated more in-depth studies into the mechanisms that lead to neurodegeneration. In just a few decades, knowledge of CCA2 and other spinocerebellar ataxias has increased significantly, facilitating the development of genetic tests and new therapeutic approaches to treatment. In parallel, it is important to note that independent studies have been conducted in different countries, confirming the existence of this disorder as a distinct category of 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>Spinocerebellar ataxia type 2 is a relatively rare disorder, with an incidence of approximately 1:100,000 to 1:200,000 of the population. Epidemiological data show that the prevalence of CCA2 may vary by region and ethnic group. For example, some populations, such as Hispanic areas, have higher rates, which may be due to a genetic predisposition. Studies show that the disease typically begins to manifest itself between the ages of 30 and 50, but cases of onset at an earlier or later age are also not uncommon. The progression of the disease may vary, making its clinical course individual and unique to each patient.<\/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_%D0%BA_%D0%B4%D0%B0%D0%BD%D0%BD%D0%BE%D0%BC%D1%83_%D0%B7%D0%B0%D0%B1%D0%BE%D0%BB%D0%B5%D0%B2%D0%B0%D0%BD%D0%B8%D1%8E\"><\/span>Genetic predisposition to this disease<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>CCA2 is caused by mutations in the ATXN2 gene, which is located on chromosome 12. The underlying mechanism of this disorder is the expansion of CAG repeats in this gene; the norm is 22-23 repeats, while in patients with CCA2 this figure exceeds 30. The increase in the number of CAG repeats leads to the production of an abnormal protein, ataxin-2, which accumulates and causes degeneration of neurons in the cerebellum and spinal cord. Genetic studies have also revealed that the presence of a mutation may not always lead to a clinical picture of the disease, indicating the presence of modifying factors, such as interactions with other genes or the environment, which requires further study.<\/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_%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>Risk factors for the development of this disease<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>Risk factors for spinocerebellar ataxia type 2 can be divided into hereditary and environmental. <\/p>\n<ul>\n<li>Hereditary: presence of a family history of the disease, presence of expanded CAG repeats in the ATXN2 gene.<\/li>\n<li>Physical factors: sedentary lifestyle, aging.<\/li>\n<li>Chemical factors: toxic effects on the nervous system, which may be associated with the environment or work with certain chemicals.<\/li>\n<li>Others: presence of comorbidities that influence neurodegeneration (eg, diabetes, cardiovascular disease).<\/li>\n<\/ul>\n<p>Thus, most risk factors are determined by genetic parameters, but external factors can also influence the manifestations of the disease and its progression.<\/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 spinocerebellar ataxia type 2 requires a comprehensive approach that includes several aspects:<\/p>\n<ul>\n<li>Main symptoms: progressive ataxia, balance disorder, sometimes eye disorders (nystagmus), dysarthria.<\/li>\n<li>Laboratory tests: genetic testing for the presence of a mutation in the ATXN2 gene, as well as tests to rule out other diseases.<\/li>\n<li>Radiological examinations: magnetic resonance imaging (MRI) to visualize changes in the cerebellum and spinal cord.<\/li>\n<li>Other types of diagnostics: neuropsychological tests to assess cognitive functions.<\/li>\n<\/ul>\n<p>An important component is the differential diagnosis, which includes the exclusion of other forms of ataxia, such as spinocerebellar ataxia type 1 or other genetically determined diseases, which requires an analysis of the clinical picture and family history of the patient.<\/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>There is currently no specific therapy for spinocerebellar ataxia type 2, but there are a number of approaches aimed at relieving symptoms and slowing the progression of the disease. Treatments can be divided into several categories:<\/p><script data-noptimize=\"\" data-wpfc-render=\"false\">\nfpm_start( \"true\" );\n<\/script>\n\n<ul>\n<li>General treatment: rehabilitation programs including physical therapy and occupational therapy to improve coordination and balance.<\/li>\n<li>Pharmacological treatment: use of neuroprotective agents such as antioxidants (eg, vitamin E), antidepressants to help cope with emotional problems.<\/li>\n<li>Surgical treatment: In rare cases, surgical interventions may be used to correct balance disorders.<\/li>\n<li>Other treatments: Therapeutic approaches such as stem cell transfusions are being investigated, but their effectiveness and safety still need to be confirmed in clinical trials.<\/li>\n<\/ul>\n<p>Each treatment plan must be individualized based on the symptoms and disease progression of the individual patient.<\/p>\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_%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>List of medications used to treat this disease<span class=\"ez-toc-section-end\"><\/span><\/h2>\n<p>There are currently no specific drugs to treat CCA2. However, some drugs may be used to relieve symptoms:<\/p>\n<ul>\n<li>Vitamin E (antioxidant)<\/li>\n<li>Selective serotonin reuptake inhibitors (SSRIs) for the treatment of depression<\/li>\n<li>Drugs for improving metabolism and neuroprotection<\/li>\n<li>Physiotherapeutic means for rehabilitation.<\/li>\n<\/ul>\n<p>However, it is important to note that the effectiveness of medications may vary and requires an individual approach.<\/p>\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 patients with spinocerebellar ataxia type 2 includes regular clinical examinations and assessment of symptom progression:<\/p>\n<ul>\n<li>Monitoring steps: regular neurological examinations for progression of ataxia and other symptoms.<\/li>\n<li>Prognosis: The course of the disease is individual; some patients can maintain independence in daily life for many years.<\/li>\n<li>Complications: Possible secondary complications due to impaired coordination, including falls and injuries, and potential breathing and swallowing problems in later stages.<\/li>\n<\/ul>\n<p>However, a competent approach to monitoring and rehabilitation can significantly improve the quality of life of patients.<\/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>Spinocerebellar ataxia type 2 can manifest itself in different age groups. As a rule, the onset of the disease occurs at the age of 30-50 years, however, cases of manifestation at an earlier or later age are also known. <\/p>\n<ul>\n<li>In young patients, the clinical course may be more acute, with rapid progression of symptoms.<\/li>\n<li>Middle-aged patients often experience a slower rate of disease progression, allowing them to maintain independent mobility for longer.<\/li>\n<li>In older people, the course of the disease may be complicated by concomitant health problems, which requires a comprehensive approach to treatment and rehabilitation.<\/li>\n<\/ul>\n<p>Treatment and monitoring approaches should be based on the patient&#039;s age and individual characteristics.<\/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>What is spinocerebellar ataxia type 2?<\/strong><br \/>\nSpinocerebellar ataxia type 2 is a hereditary disorder characterized by progressive ataxia and coordination problems associated with mutations in the ATXN2 gene.<\/li>\n<li><strong>How is CCA2 diagnosed?<\/strong><br \/>\nDiagnosis includes genetic testing, MRI, tests to rule out other diseases, and evaluation of neurological symptoms.<\/li>\n<li><strong>What is the treatment for spinocerebellar ataxia type 2?<\/strong><br \/>\nTreatment includes rehabilitation, drug therapy to manage symptoms, and, in some cases, surgery.<\/li>\n<li><strong>What are the risk factors for developing CCA2?<\/strong><br \/>\nRisk factors include a family history of the disease, genetic mutations, and physical and chemical factors.<\/li>\n<li><strong>What is the prognosis for patients with CCA2?<\/strong><br \/>\nThe prognosis varies; some patients may remain independent for a long time, while others may experience rapid disease progression.<\/li>\n<\/ul>\n<div class=\"fpm_end\"><\/div>","protected":false},"excerpt":{"rendered":"<p>Spinocerebellar ataxia type 2 (SCA2) is an inherited neurodegenerative disorder characterized by progressive ataxia, impaired motor coordination, and other<\/p>","protected":false},"author":1,"featured_media":23317,"comment_status":"open","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[298],"tags":[],"class_list":["post-13063","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\/13063","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=13063"}],"version-history":[{"count":1,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/posts\/13063\/revisions"}],"predecessor-version":[{"id":13857,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/posts\/13063\/revisions\/13857"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/media\/23317"}],"wp:attachment":[{"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/media?parent=13063"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/categories?post=13063"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/valintermed.com\/en\/wp-json\/wp\/v2\/tags?post=13063"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}