{"id":6571,"date":"2026-03-30T11:00:41","date_gmt":"2026-03-30T11:00:41","guid":{"rendered":"https:\/\/yourprofitbeacon.com\/index.php\/2026\/03\/30\/discovery-offers-hope-to-children-with-rare-and-severe-epilepsy\/"},"modified":"2026-03-30T11:00:41","modified_gmt":"2026-03-30T11:00:41","slug":"discovery-offers-hope-to-children-with-rare-and-severe-epilepsy","status":"publish","type":"post","link":"https:\/\/yourprofitbeacon.com\/index.php\/2026\/03\/30\/discovery-offers-hope-to-children-with-rare-and-severe-epilepsy\/","title":{"rendered":"Discovery offers hope to children with rare and severe epilepsy"},"content":{"rendered":"<p>Scientists say they have discovered a new condition behind one of the most common genetic causes of severe epilepsy in children.<\/p>\n<p>The condition &#8211; named recessive RNU2-2-related neurodevelopmental disorder &#8211; leads to seizures and severe developmental delays before children are a year old.<\/p>\n<p>Experts estimate millions of people could be carriers of the faulty gene behind the disorder.<\/p>\n<p>Children with the condition suffer seizures that can cause them to jerk, stiffen, shake and lose consciousness.<\/p>\n<p>It can also take them longer to learn to walk and talk, and sufferers may have significant learning problems.<\/p>\n<p>Researchers from the University of Manchester and <strong>Manchester<\/strong> University NHS Foundation Trust analysed changes in several hundred RNU genes in people involved in the 100,000 Genomes Project.<\/p>\n<p>Eighty-four people, including five-year-old Ava Begley from Sydney, Australia, have so far been identified as having the new condition &#8211; with many more believed to be undiagnosed around the world.<\/p>\n<p>The Manchester researchers and the Sydney Children&#8217;s Hospital Clinical Genetics Team helped link Ava&#8217;s condition to the RNU2-2-related disorder.<\/p>\n<p>Ava is non-verbal and has complex neurological symptoms, and suffers frequent seizures due to her severe epilepsy. She used to have 100 to 200 seizures a day, but these are now more controlled thanks to medication.<\/p>\n<p>Her parents said they were relieved to finally have a diagnosis but also sad &#8220;in understanding the seriousness of the condition and how rare it is&#8221;.<\/p>\n<p>&#8220;It gives Ava a name and a place in the medical world, rather than being an unanswered mystery,&#8221; they said in a statement.<\/p>\n<p>&#8220;It helps us feel that we are getting closer to the starting point of being able to find a cure\/treatment, and provides hope that research and awareness may lead to better understanding and support in the future.&#8221;<\/p>\n<p>The findings have been published in the journal Nature Genetics and study lead Adam Jackson said it is believed &#8220;as many as one in 100 people could unknowingly be carriers of this condition&#8221;.<\/p>\n<p>Dr Jackson, from the Manchester Centre for Genomic Medicine, said: &#8220;If both parents are carriers, there is a one in four chance with every pregnancy that their child could be affected.<\/p>\n<p>&#8220;We estimate roughly one in 40,000 people may be living with this condition, making it one of the most common neurodevelopmental disorders currently known.&#8221;<\/p>\n<p>&#8220;Unlike most other genes, RNU2-2 does not even make a protein,&#8221; Dr Jackson added.<\/p>\n<p>&#8220;We were astonished to discover how changes in this tiny gene can have such profound effects in so many individuals.&#8221;<\/p>\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Scientists say they have discovered a new condition behind one of the most common genetic causes of severe epilepsy in children. The condition &#8211; named recessive RNU2-2-related neurodevelopmental disorder &#8211; leads to seizures and severe developmental delays before children are a year old. Experts estimate millions of people could be carriers of the faulty gene [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":6572,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2],"tags":[],"class_list":["post-6571","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-techscience"],"_links":{"self":[{"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/posts\/6571","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/comments?post=6571"}],"version-history":[{"count":0,"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/posts\/6571\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/media\/6572"}],"wp:attachment":[{"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/media?parent=6571"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/categories?post=6571"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/yourprofitbeacon.com\/index.php\/wp-json\/wp\/v2\/tags?post=6571"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}