Shelmerdine Susan Cheng, Brittain Helen, Arthurs Owen J, Calder Alistair D
Department of Diagnostic Imaging, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Radiology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
Am J Med Genet A. 2016 Aug;170(8):2039-43. doi: 10.1002/ajmg.a.37776. Epub 2016 Jun 3.
Achondroplasia is the most common form of short limb dwarfism in humans. The shortening of the limb lengths in achondroplasia is widely described as "rhizomelic." While this appearance may be convincing clinically, the description is not necessarily true or helpful radiologically. The aims of this study, were therefore, to determine whether rhizomelic shortening is a true feature of achondroplasia at diagnosis in infancy. Humeral, radial, femoral, and tibial diaphyseal lengths were recorded by two independent observers from 22 skeletal surveys of infants with achondroplasia and compared with 150 normal age-matched control subjects. Upper and lower limb bone length ratios (radial/humeral and tibial/femoral lengths, respectively) in both groups were compared using an unpaired t-test. Mean upper limb length ratios were statistically higher within the achondroplasia group at 0.87 ± 0.04 (n = 22, mean age 70 ± 94 days) compared to normal controls at 0.79 ± 0.02 (n = 150, mean age 113 days ± 88 days; P < 0.0001). Lower limb length ratios were not significantly different between groups (0.84 ± 0.04 vs. 0.83 ± 0.02, P = 0.46). There was good inter-observer agreement of limb length measurements, with an average measurement difference of 0.1 ± 1.4 mm. In conclusion, infants with achondroplasia demonstrate statistically significant rhizomelic shortening within the upper limbs, but not lower limbs at diagnosis, compared to normal controls. The term "rhizomelic shortening" in relation to achondroplasia should be reserved when describing upper limb proportions. © 2016 Wiley Periodicals, Inc.
软骨发育不全是人类短肢侏儒症最常见的形式。软骨发育不全中四肢长度的缩短在临床上广泛被描述为“近侧短小”。虽然这种表现临床上可能令人信服,但从放射学角度来看,这种描述不一定正确或有用。因此,本研究的目的是确定近侧短小是否是婴儿期诊断软骨发育不全的一个真实特征。两名独立观察者记录了22例软骨发育不全婴儿骨骼检查的肱骨、桡骨、股骨和胫骨干长度,并与150名年龄匹配的正常对照受试者进行比较。使用不成对t检验比较两组的上肢和下肢骨长度比(分别为桡骨/肱骨和胫骨/股骨长度)。软骨发育不全组的平均上肢长度比在统计学上高于正常对照组,软骨发育不全组为0.87±0.04(n = 22,平均年龄70±94天),正常对照组为0.79±0.02(n = 150,平均年龄113天±88天;P < 0.0001)。两组间下肢长度比无显著差异(0.84±0.04对0.83±0.02,P = 0.46)。观察者之间四肢长度测量的一致性良好,平均测量差异为0.1±1.4毫米。总之,与正常对照组相比,软骨发育不全婴儿在诊断时上肢存在统计学上显著的近侧短小,而下肢则不存在。在描述上肢比例时,应保留与软骨发育不全相关的“近侧短小”一词。© 2016威利期刊公司