Donnelly Deirdre E, McConnell Vivienne, Paterson Anne, Morrison Patrick J
Department of Clinical Genetics, Belfast HSC Trust, Belfast, BT9 7AB, United Kingdom.
Ulster Med J. 2010 Sep;79(3):114-8.
The minimum prevalence of lethal Osteogenesis imperfecta type II, thanatophoric dysplasia and achondroplasia were derived following detailed case note review of all perinatal lethal skeletal dysplasias (SD) in Northern Ireland over a 12 year period. Multiple sources of ascertainment, including genetic notes, radiological reports and post mortem findings, were used. 39 cases were identified. Thanatophoric dysplasia was the commonest diagnosis made (22), followed by osteogenesis imperfecta type II (four children) and achondroplasia (two children). Eleven other diagnoses each occurred once in the 12 year period. The minimum prevalence range, per live births, of each of the common skeletal dysplasias in Northern Ireland has been calculated; thanatophoric dysplasia 0.80/10,000, osteogenesis imperfecta type II 0.15/10,000 and achondroplasia 0.07/10,000. The prevalence range for thanatophoric dysplasia is much higher than reported in previous studies. We discuss reasons for the prevalence figures obtained.
通过对北爱尔兰12年间所有围产期致死性骨骼发育不良(SD)病例记录进行详细审查,得出了致死性II型成骨不全、致死性骨发育不全和软骨发育不全的最低患病率。使用了多种确诊来源,包括基因记录、放射学报告和尸检结果。共识别出39例病例。致死性骨发育不全是最常见的诊断(22例),其次是II型成骨不全(4例儿童)和软骨发育不全(2例儿童)。在这12年期间,其他11种诊断各出现1次。已计算出北爱尔兰每种常见骨骼发育不良在每例活产中的最低患病率范围;致死性骨发育不全为0.80/10000,II型成骨不全为0.15/10000,软骨发育不全为0.07/10000。致死性骨发育不全的患病率范围远高于以往研究报告的结果。我们讨论了得出这些患病率数据的原因。