Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation. Issue 10 (10th October 2012)

• Record Type: Journal Article
• Authors: Shaheen, Ranad; Alazami, Anas M; Alshammari, Muneera J; Faqeih, Eissa; Alhashmi, Nadia; Mousa, Noon; Alsinani, Aisha; Ansari, Shinu; Alzahrani, Fatema; Al-Owain, Mohammed; Alzayed, Zayed S; Alkuraya, Fowzan S
• Is Part Of: Journal of medical genetics. Volume 49:Issue 10(2012)
• Page Start: 630
• Page End: 635
• Publication Date: 2012-10-10
• Subjects: autosomal recessive osteogenesis imperfecta -- autozygome -- exome; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmedgenet-2012-101142
• Languages: English
• ISSNs: 1468-6244

Abstract

Abstract : Background: Osteogenesis imperfecta (OI) is an hereditary bone disease in which increased bone fragility leads to frequent fractures and other complications, usually in an autosomal dominant fashion. An expanding list of genes that encode proteins related to collagen metabolism are now recognised as important causes of autosomal recessive (AR) OI. Our aim was to study the contribution of known genes to AR OI in order to identify novel loci in mutation-negative cases. Methods: We enrolled multiplex consanguineous families and simplex cases (also consanguineous) in which mutations in COL1A1 and COL1A2 had been excluded. We used autozygome guided mutation analysis of AR OI (AR OI) genes followed by exome sequencing when such analysis failed to identify the causative mutation. Results: Two simplex and 11 multiplex families were enrolled, encompassing 27 cases. In three multiplex families, autozygosity and linkage analysis revealed a novel recessive OI locus on chromosome 9q31.1-31.3, and a novel truncating deletion of exon 4 of TMEM38B was identified within that interval. In addition, gonadal or gonadal/somatic mosaic mutations in COL1A1 or COL1A2 and homozygous mutations in recently described AR OI genes were identified in all remaining families. Conclusions: TMEM38B is a novel candidate gene for AR OI. Future studies are needed to explore fully the contribution of this gene to AR OI in other populations.