{"id":1116,"date":"2018-03-07T19:35:12","date_gmt":"2018-03-07T19:35:12","guid":{"rendered":"https:\/\/blogs.bmj.com\/jmg\/?p=1116"},"modified":"2026-02-24T15:56:32","modified_gmt":"2026-02-24T15:56:32","slug":"homozygous-chst11-mutation-in-chondrodysplasia-brachydactyly-overriding-digits-clino-symphalangism-and-synpolydactyly","status":"publish","type":"post","link":"https:\/\/blogs.bmj.com\/jmg\/2018\/03\/07\/homozygous-chst11-mutation-in-chondrodysplasia-brachydactyly-overriding-digits-clino-symphalangism-and-synpolydactyly\/","title":{"rendered":"Homozygous CHST11 mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactyly (Contributed by Dr. Asl\u0131 Tolun)"},"content":{"rendered":"<p>In a Pakistani family with limb malformations that include short fingers, cross fingers, fused fingers, fused finger bones, fused toes and supernumerary toes plus skeletal defects that include scoliosis, dislocated patellae and fibulae and pectus excavatum, we identified the underlying mutation as a homozygous five-amino acid deletion in protein CHST11. Our findings confirm the crucial role of CHST11 in skeletal morphogenesis and show that CHST11 defects have variable phenotypic manifestations that include a variety of limb malformations and skeletal defects. Also, elder patients had symptoms of arthritis, concordant with studies that have identified CHST11 locus as a susceptibility locus for osteoarthritis. (<a href=\"http:\/\/jmg.bmj.com\/content\/early\/2018\/03\/07\/jmedgenet-2017-105003\">http:\/\/jmg.bmj.com\/content\/early\/2018\/03\/07\/jmedgenet-2017-105003<\/a> )<\/p>\n<p><a href=\"https:\/\/blogs.bmj.com\/jmg\/files\/2018\/03\/JMG-Jan-18.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1117\" src=\"https:\/\/blogs.bmj.com\/jmg\/files\/2018\/03\/JMG-Jan-18-300x225.jpg\" alt=\"\" width=\"300\" height=\"225\" srcset=\"https:\/\/blogs.bmj.com\/jmg\/files\/2018\/03\/JMG-Jan-18-300x225.jpg 300w, https:\/\/blogs.bmj.com\/jmg\/files\/2018\/03\/JMG-Jan-18-768x576.jpg 768w, https:\/\/blogs.bmj.com\/jmg\/files\/2018\/03\/JMG-Jan-18-1024x768.jpg 1024w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n<p>Dr. Asl\u0131 Tolun&#8217;s group<!--TrendMD v2.4.8--><\/p>\n","protected":false},"excerpt":{"rendered":"<p>In a Pakistani family with limb malformations that include short fingers, cross fingers, fused fingers, fused finger bones, fused toes and supernumerary toes plus skeletal defects that include scoliosis, dislocated patellae and fibulae and pectus excavatum, we identified the underlying mutation as a homozygous five-amino acid deletion in protein CHST11. Our findings confirm the crucial [&#8230;]<\/p>\n<p><a class=\"btn btn-secondary understrap-read-more-link\" href=\"https:\/\/blogs.bmj.com\/jmg\/2018\/03\/07\/homozygous-chst11-mutation-in-chondrodysplasia-brachydactyly-overriding-digits-clino-symphalangism-and-synpolydactyly\/\">Read More&#8230;<\/a><\/p>\n","protected":false},"author":123,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-1116","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Homozygous CHST11 mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactyly (Contributed by Dr. Asl\u0131 Tolun) - JMG Contact blog<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/blogs.bmj.com\/jmg\/2018\/03\/07\/homozygous-chst11-mutation-in-chondrodysplasia-brachydactyly-overriding-digits-clino-symphalangism-and-synpolydactyly\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Homozygous CHST11 mutation in chondrodysplasia, brachydactyly, overriding digits, clino-symphalangism and synpolydactyly (Contributed by Dr. Asl\u0131 Tolun) - JMG Contact blog\" \/>\n<meta property=\"og:description\" content=\"In a Pakistani family with limb malformations that include short fingers, cross fingers, fused fingers, fused finger bones, fused toes and supernumerary toes plus skeletal defects that include scoliosis, dislocated patellae and fibulae and pectus excavatum, we identified the underlying mutation as a homozygous five-amino acid deletion in protein CHST11. 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