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An Unusual Association: Silver-Russell Syndrome and Ectopic Thyroid.一种罕见的关联:Silver-Russell综合征与异位甲状腺。
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Genomic imprinting and the evolutionary psychology of human kinship.基因组印迹与人类亲属关系的进化心理学。
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Growth hormone therapy in Silver Russell syndrome: 5 years experience of the Australian and New Zealand Growth database (OZGROW).Silver-Russell综合征的生长激素治疗:澳大利亚和新西兰生长数据库(OZGROW)的5年经验
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本文引用的文献

1
Application of the Gompertz curve to the observed pattern of growth in length of 48 individual boys and girls during the adolescent cycle of growth.将冈珀茨曲线应用于48名个体男孩和女孩在青春期生长周期中观察到的身高增长模式。
Hum Biol. 1957 Feb;29(1):83-122.
2
A syndrome of intra-uterine dwarfism recognizable at birth with cranio-facial dysostosis, disproportionately short arms, and other anomalies (5 examples).一种出生时即可识别的宫内侏儒综合征,伴有颅面骨发育不全、手臂不成比例地短小及其他异常(5例)。
Proc R Soc Med. 1954 Dec;47(12):1040-4.
3
Syndrome of congenital hemihypertrophy, shortness of stature, and elevated urinary gonadotropins.先天性半侧肥大、身材矮小及尿促性腺激素升高综合征。
Pediatrics. 1953 Oct;12(4):368-76.
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Variations in pattern of pubertal changes in girls.女孩青春期变化模式的差异。
Arch Dis Child. 1969 Jun;44(235):291-303. doi: 10.1136/adc.44.235.291.
5
Standards for birthweight as gestation periods from 32 to 42 weeks, allowing for maternal height and weight.32至42周孕期的出生体重标准,考虑了母亲的身高和体重。
Arch Dis Child. 1970 Aug;45(242):566-9. doi: 10.1136/adc.45.242.566.
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Variations in the pattern of pubertal changes in boys.男孩青春期变化模式的差异。
Arch Dis Child. 1970 Feb;45(239):13-23. doi: 10.1136/adc.45.239.13.
7
Effect of human growth hormone treatment for 1 to 7 years on growth of 100 children, with growth hormone deficiency, low birthweight, inherited smallness, Turner's syndrome, and other complaints.对100名患有生长激素缺乏症、低出生体重、遗传性身材矮小、特纳综合征及其他病症的儿童进行1至7年生长激素治疗的效果
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[Natural history of intrauterine growth retardation: pubertal growth and adult height].宫内生长迟缓的自然史:青春期生长及成人身高
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Intrauterine growth retardation and early adolescent growth spurt in two sisters.
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Silver-Russell综合征中的青少年生长与青春期发育进程

Adolescent growth and pubertal progression in the Silver-Russell syndrome.

作者信息

Davies P S, Valley R, Preece M A

机构信息

Department of Growth and Development, Institute of Child Health, London.

出版信息

Arch Dis Child. 1988 Feb;63(2):130-5. doi: 10.1136/adc.63.2.130.

DOI:10.1136/adc.63.2.130
PMID:3348659
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1778748/
Abstract

The pattern of growth and development of 18 adolescent children with the Silver-Russell syndrome was studied. Mature height was about -3.6 standard deviation scores in both sexes. This is comparable to the height reduction at diagnosis, which has been reported previously. The pattern of puberty and adolescent growth was essentially normal and occurred at a marginally earlier time than normal, although in this small series the differences were not significant. In the girls there was a tendency to gain subcutaneous fat after puberty. This trend was not apparent in the boys.

摘要

对18名患有Silver-Russell综合征的青少年儿童的生长发育模式进行了研究。两性的成熟身高均约为-3.6标准差分数。这与先前报道的诊断时的身高降低情况相当。青春期和青少年生长模式基本正常,且比正常情况略早出现,不过在这个小样本系列中,差异并不显著。在女孩中,青春期后有增加皮下脂肪的趋势。这种趋势在男孩中不明显。