{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,20]],"date-time":"2026-01-20T10:50:12Z","timestamp":1768906212113,"version":"3.49.0"},"reference-count":45,"publisher":"BMJ","issue":"10","license":[{"start":{"date-parts":[[2023,5,16]],"date-time":"2023-05-16T00:00:00Z","timestamp":1684195200000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"name":"Instituto de Salud Carlos III, Spain","award":["CP22\/00141"],"award-info":[{"award-number":["CP22\/00141"]}]},{"name":"European Regional Development Fund (ERDF) \u201cA way to achieve Europe\u201d","award":["PI19\/00122"],"award-info":[{"award-number":["PI19\/00122"]}]},{"DOI":"10.13039\/501100004587","name":"Instituto de Salud Carlos III","doi-asserted-by":"publisher","award":["FI21\/0073"],"award-info":[{"award-number":["FI21\/0073"]}],"id":[{"id":"10.13039\/501100004587","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["bmj.com"],"crossmark-restriction":true},"short-container-title":["J Med Genet"],"accepted":{"date-parts":[[2023,3,28]]},"published-print":{"date-parts":[[2023,10]]},"abstract":"<jats:sec>\n                  <jats:title>Background<\/jats:title>\n                  <jats:p>Limb-girdle muscular dystrophies (LGMD) are a heterogeneous group of genetically determined muscle disorders. TRAPPC11-related LGMD is an autosomal-recessive condition characterised by muscle weakness and intellectual disability.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods<\/jats:title>\n                  <jats:p>A clinical and histopathological characterisation of 25 Roma individuals with LGMD R18 caused by the homozygous <jats:italic>TRAPPC11<\/jats:italic> c.1287+5G&gt;A variant is reported. Functional effects of the variant on mitochondrial function were investigated.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Results<\/jats:title>\n                  <jats:p>The c.1287+5G&gt;A variant leads to a phenotype characterised by early onset muscle weakness, movement disorder, intellectual disability and elevated serum creatine kinase, which is similar to other series. As novel clinical findings, we found that microcephaly is almost universal and that infections in the first years of life seem to act as triggers for a psychomotor regression and onset of seizures in several individuals with <jats:italic>TRAPPC11<\/jats:italic> variants, who showed pseudometabolic crises triggered by infections. Our functional studies expanded the role of TRAPPC11 deficiency in mitochondrial function, as a decreased mitochondrial ATP production capacity and alterations in the mitochondrial network architecture were detected.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusion<\/jats:title>\n                  <jats:p>We provide a comprehensive phenotypic characterisation of the pathogenic variant <jats:italic>TRAPPC11<\/jats:italic> c.1287+5G&gt;A, which is founder in the Roma population. Our observations indicate that some typical features of golgipathies, such as microcephaly and clinical decompensation associated with infections, are prevalent in individuals with LGMD R18.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1136\/jmg-2022-109132","type":"journal-article","created":{"date-parts":[[2023,5,17]],"date-time":"2023-05-17T03:21:24Z","timestamp":1684293684000},"page":"965-973","update-policy":"https:\/\/doi.org\/10.1136\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":11,"title":["Expanding the phenotypic spectrum of <i>TRAPPC11-<\/i>related muscular dystrophy: 25 Roma individuals carrying a founder variant"],"prefix":"10.1136","volume":"60","author":[{"given":"Maria","family":"Justel","sequence":"first","affiliation":[{"name":"Neuromuscular Unit, Department of Neurology, Hospital Sant Joan de D\u00e9u, Barcelona, Spain"},{"name":"Department of Paediatrics, Complejo asistencial de Salamanca, Salamanca, 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