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Am J Med Genet. 1987 Feb;26(2):445-55. doi: 10.1002/ajmg.1320260224.
2
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本文引用的文献

1
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.15号染色体异常与普拉德-威利综合征:40例随访报告
Am J Hum Genet. 1982 Mar;34(2):278-85.
2
Anthropometry and numerical taxonomy in clinical genetics: an example of applied biological anthropology.
Am J Phys Anthropol. 1984 Jun;64(2):147-54. doi: 10.1002/ajpa.1330640208.
3
Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.15号染色体异常与普拉德-威利综合征:细胞遗传学分析
Hum Genet. 1984;66(4):313-34. doi: 10.1007/BF00287636.
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Parental origin of chromosome 15 deletion in Prader-Willi syndrome.普拉德-威利综合征中15号染色体缺失的亲本来源
Lancet. 1983 Jun 4;1(8336):1285-6. doi: 10.1016/s0140-6736(83)92745-9.
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Skinfolds, body girths, biacromial diameter, and selected anthropometric indices of adults. United States, 1960-1962.成年人的皮褶厚度、身体围度、肩峰间径及选定的人体测量指标。美国,1960年至1962年。
Vital Health Stat 11. 1970 Feb(35):1-63.
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7
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8
Triceps skin fold and upper arm muscle size norms for assessment of nutrition status.用于评估营养状况的肱三头肌皮褶厚度和上臂肌肉大小标准。
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9
Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome. A follow-up report on 38 cases.普拉德-威利综合征的掌指纹型分析。38例随访报告。
Clin Genet. 1985 Jul;28(1):27-30. doi: 10.1111/j.1399-0004.1985.tb01213.x.
10
Revised standards for triceps and subscapular skinfolds in British children.英国儿童肱三头肌及肩胛下皮褶厚度的修订标准
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一项针对38名普拉德-威利综合征患者的人体测量学研究。

An anthropometric study of 38 individuals with Prader-Labhart-Willi syndrome.

作者信息

Butler M G, Meaney F J

出版信息

Am J Med Genet. 1987 Feb;26(2):445-55. doi: 10.1002/ajmg.1320260224.

DOI:10.1002/ajmg.1320260224
PMID:3812595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5482271/
Abstract

Weight, height, sitting height, and 24 other anthropometric variables (5 body circumferences, skinfolds at 7 sites, 4 head dimensions, and 8 hand and foot measurements) were obtained on 38 Prader-Labhart-Willi syndrome (PLWS) individuals (21 with apparent chromosome 15 deletions and 17 nondeletion cases) with an age range of 2 weeks to 38 1/2 years. More than half of these individuals were measured on more than one occasion. The measurements confirmed the presence of short stature, small hands and feet, obesity, and narrow bi-frontal diameter in PLWS. No differences were found for the anthropometric measurements between the 2 chromosome subgroups. Inverse correlations were produced with linear measurements (eg, height, hand and foot lengths) and age, which indicated a deceleration of linear growth relative to normal individuals with increasing age.

摘要

对38名普拉德-拉巴尔特-威利综合征(PLWS)患者(21例有明显的15号染色体缺失,17例无缺失)进行了体重、身高、坐高以及其他24项人体测量变量(5项身体周长、7个部位的皮褶厚度、4项头部尺寸以及8项手足测量)的测量,年龄范围为2周龄至38.5岁。这些个体中超过一半接受了不止一次测量。测量结果证实PLWS患者存在身材矮小、手足短小、肥胖以及双额径狭窄的情况。两个染色体亚组之间的人体测量结果未发现差异。线性测量值(如身高、手足长度)与年龄呈负相关,这表明随着年龄增长,相对于正常个体,线性生长减速。