Department of Pediatric Genetics, Amrita Institute of Medical Sciences & Research Centre, Cochin, Kerala, India.
Department of Biomolecular Medicine, Center for Medical Genetics Ghent, Ghent University Hospital, Ghent, Belgium.
Am J Med Genet A. 2019 Jun;179(6):908-914. doi: 10.1002/ajmg.a.61119. Epub 2019 Mar 21.
Osteogenesis imperfecta (OI) is a heritable connective tissue disorder, mainly characterized by bone fragility and low bone mass. Defects in the type I procollagen-encoding genes account for the majority of OI, but increasingly more rare autosomal recessive (AR) forms are being identified, which are caused by defects in genes involved in collagen metabolism, bone mineralization, or osteoblast differentiation. Bi-allelic mutations in WNT1 have been associated with a rare form of AR OI, characterized by severe osteoporosis, vertebral compression, scoliosis, fractures, short stature, and variable neurological problems. Heterozygous WNT1 mutations have been linked to autosomal dominant early-onset osteoporosis. In this study, we describe the clinical and molecular findings in 10 new patients with AR WNT1-related OI. Thorough revision of the clinical symptoms of these 10 novel patients and previously published AR WNT1 OI cases highlight ptosis as a unique hallmark in the diagnosis of this OI subtype.
成骨不全症(OI)是一种遗传性结缔组织疾病,主要特征为骨骼脆弱和低骨量。I 型前胶原编码基因的缺陷占 OI 的大多数,但越来越多的罕见常染色体隐性(AR)形式被确定,这些形式是由涉及胶原代谢、骨矿化或成骨细胞分化的基因缺陷引起的。WNT1 的双等位基因突变与一种罕见的 AR OI 相关,其特征为严重的骨质疏松症、椎体压缩、脊柱侧凸、骨折、身材矮小和可变的神经问题。WNT1 的杂合突变与常染色体显性早发性骨质疏松症有关。在这项研究中,我们描述了 10 名新的 AR WNT1 相关 OI 患者的临床和分子发现。对这 10 名新患者和以前发表的 AR WNT1 OI 病例的临床症状进行彻底回顾,强调了上睑下垂是这种 OI 亚型诊断的独特特征。