{"id":1825,"date":"2023-01-13T15:58:23","date_gmt":"2023-01-13T15:58:23","guid":{"rendered":"https:\/\/blogs.bmj.com\/jmg\/?p=1825"},"modified":"2026-02-23T00:19:53","modified_gmt":"2026-02-23T00:19:53","slug":"biallelic-frameshift-variants-in-phldb1-cause-mild-type-osteogenesis-imperfecta-with-regressive-spondylometaphyseal-changes","status":"publish","type":"post","link":"https:\/\/blogs.bmj.com\/jmg\/2023\/01\/13\/biallelic-frameshift-variants-in-phldb1-cause-mild-type-osteogenesis-imperfecta-with-regressive-spondylometaphyseal-changes\/","title":{"rendered":"Biallelic frameshift variants in PHLDB1 cause mild type Osteogenesis Imperfecta with regressive spondylometaphyseal changes (Contributed by Prof. Beyhan T\u00fcys\u00fcz)"},"content":{"rendered":"<p>Osteogenesis imperfecta (OI) is a group of disorders, mostly autosomal dominant, inherited characterized by susceptibility to fractures, resulting from a type 1 collagen defect. Although many autosomal recessive genes have been shown to cause OI in recent years, there are still patients whose molecular defect is still unknown. In this study, we described recurrent fractures, bluish sclerae, bowing of lower limbs and short stature in five infants from two unrelated Turkish families. Two different homozigous pathogenic variants, in a novel candidate gene, <em>PHLDB1<\/em>, were shown to cause this mild OI phenotype in these families. The demonstration of decreased PHLDB1 mRNA expression levels in blood and fibroblast samples with different pathogenic variants supported the hypothesis that these variants were causative for the observed phenotype. (<a href=\"https:\/\/jmg.bmj.com\/content\/early\/2022\/12\/21\/jmg-2022-108763\">https:\/\/jmg.bmj.com\/content\/early\/2022\/12\/21\/jmg-2022-108763<\/a> )<\/p>\n<p><a href=\"https:\/\/blogs.bmj.com\/jmg\/2023\/01\/13\/biallelic-frameshift-variants-in-phldb1-cause-mild-type-osteogenesis-imperfecta-with-regressive-spondylometaphyseal-changes\/picture2\/\" rel=\"attachment wp-att-1826\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-1826\" src=\"https:\/\/blogs.bmj.com\/jmg\/files\/2023\/01\/Picture2-300x230.jpg\" alt=\"\" width=\"300\" height=\"230\" srcset=\"https:\/\/blogs.bmj.com\/jmg\/files\/2023\/01\/Picture2-300x230.jpg 300w, https:\/\/blogs.bmj.com\/jmg\/files\/2023\/01\/Picture2-640x491.jpg 640w, https:\/\/blogs.bmj.com\/jmg\/files\/2023\/01\/Picture2.jpg 653w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/a><\/p>\n<p>Beyhan T\u00fcys\u00fcz and Dilek Uluda\u011f Alkaya\u00a0 with some co-authors at Istanbul University-Cerrahpasa, Cerrahpasa Medical School<!--TrendMD v2.4.8--><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Osteogenesis imperfecta (OI) is a group of disorders, mostly autosomal dominant, inherited characterized by susceptibility to fractures, resulting from a type 1 collagen defect. Although many autosomal recessive genes have been shown to cause OI in recent years, there are still patients whose molecular defect is still unknown. In this study, we described recurrent fractures, [&#8230;]<\/p>\n<p><a class=\"btn btn-secondary understrap-read-more-link\" href=\"https:\/\/blogs.bmj.com\/jmg\/2023\/01\/13\/biallelic-frameshift-variants-in-phldb1-cause-mild-type-osteogenesis-imperfecta-with-regressive-spondylometaphyseal-changes\/\">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-1825","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Biallelic frameshift variants in PHLDB1 cause mild type Osteogenesis Imperfecta with regressive spondylometaphyseal changes (Contributed by Prof. Beyhan T\u00fcys\u00fcz) - 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\/2023\/01\/13\/biallelic-frameshift-variants-in-phldb1-cause-mild-type-osteogenesis-imperfecta-with-regressive-spondylometaphyseal-changes\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Biallelic frameshift variants in PHLDB1 cause mild type Osteogenesis Imperfecta with regressive spondylometaphyseal changes (Contributed by Prof. Beyhan T\u00fcys\u00fcz) - JMG Contact blog\" \/>\n<meta property=\"og:description\" content=\"Osteogenesis imperfecta (OI) is a group of disorders, mostly autosomal dominant, inherited characterized by susceptibility to fractures, resulting from a type 1 collagen defect. Although many autosomal recessive genes have been shown to cause OI in recent years, there are still patients whose molecular defect is still unknown. 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