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Does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially?生长激素治疗对患有和未患线粒体疾病的患者的影响是否存在差异？
Clin Pediatr Endocrinol. 2018;27(2):107-108. doi: 10.1297/cpe.27.107. Epub 2018 Apr 13.
2
Pycnodysostosis: clinical, radiologic, and endocrine evaluation and linear growth after growth hormone therapy.致密性成骨不全症：生长激素治疗后的临床、放射学及内分泌评估与线性生长
Metabolism. 2001 Aug;50(8):905-11. doi: 10.1053/meta.2001.24924.
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Growth hormone treatment of idiopathic short stature.生长激素治疗特发性身材矮小症。
Horm Res. 1996;46(4-5):208-14. doi: 10.1159/000185025.
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Causes of short stature in Pakistani children found at an Endocrine Center.在一家内分泌中心发现的巴基斯坦儿童身材矮小的原因。
Pak J Med Sci. 2016 Nov-Dec;32(6):1321-1325. doi: 10.12669/pjms.326.11077.
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Clinical diagnoses of children with extremely short stature and their response to growth hormone.身材极矮小儿童的临床诊断及其对生长激素的反应。
J Pediatr. 1993 May;122(5 Pt 1):687-92. doi: 10.1016/s0022-3476(06)80005-3.
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Short stature and decreased insulin-like growth factor I (IGF-I)/growth hormone (GH)-ratio in an adult GH-deficient patient pointing to additional partial GH insensitivity due to a R179C mutation of the growth hormone receptor.一名成年生长激素缺乏患者身材矮小且胰岛素样生长因子I（IGF-I）/生长激素（GH）比值降低，提示由于生长激素受体的R179C突变导致额外的部分生长激素不敏感。
Growth Horm IGF Res. 2007 Aug;17(4):307-14. doi: 10.1016/j.ghir.2007.03.001. Epub 2007 Apr 25.
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Mutations of the growth hormone receptor in children with idiopathic short stature. The Growth Hormone Insensitivity Study Group.特发性身材矮小儿童生长激素受体的突变。生长激素不敏感研究组。
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Short stature and failure of pubertal development in thalassaemia major: evidence for hypothalamic neurosecretory dysfunction of growth hormone secretion and defective pituitary gonadotropin secretion.重型地中海贫血患者的身材矮小和青春期发育迟缓：生长激素分泌的下丘脑神经分泌功能障碍及垂体促性腺激素分泌缺陷的证据。
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Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry.对国际范可尼贫血登记处转诊患者的生长和激素状态评估。
Pediatrics. 2001 Apr;107(4):744-54. doi: 10.1542/peds.107.4.744.

引用本文的文献

1
Responses to the Letter to the Editor "Does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially ?" (Vol. 27, No. 2, p. 107-108, 2018).对致编辑的信《生长激素治疗对有无线粒体疾病的患者的影响是否不同？》（《第27卷，第2期，第107 - 108页，2018年》）的回复
Clin Pediatr Endocrinol. 2018;27(3):201-202. doi: 10.1297/cpe.27.201. Epub 2018 Jul 31.

本文引用的文献

1
Incidence of diabetes mellitus and neoplasia in Japanese short-statured children treated with growth hormone in the Genetics and Neuroendocrinology of Short Stature International Study (GeNeSIS).矮小症国际研究（GeNeSIS）中接受生长激素治疗的日本矮小儿童的糖尿病和肿瘤发病率。
Clin Pediatr Endocrinol. 2017;26(4):229-241. doi: 10.1297/cpe.26.229. Epub 2017 Sep 28.
2
Clinical and Molecular Characteristics in 100 Chinese Pediatric Patients with m.3243A>G Mutation in Mitochondrial DNA.100例线粒体DNA m.3243A>G突变中国儿科患者的临床和分子特征
Chin Med J (Engl). 2016 Aug 20;129(16):1945-9. doi: 10.4103/0366-6999.187845.
3
Prevalence of neoplasms in definite and probable mitochondrial disorders.确诊和疑似线粒体疾病中肿瘤的患病率。
Mitochondrion. 2016 Jul;29:31-4. doi: 10.1016/j.mito.2016.05.002. Epub 2016 May 13.
4
Mutation in the nuclear-encoded mitochondrial isoleucyl-tRNA synthetase IARS2 in patients with cataracts, growth hormone deficiency with short stature, partial sensorineural deafness, and peripheral neuropathy or with Leigh syndrome.患有白内障、生长激素缺乏伴身材矮小、部分感音神经性耳聋和周围神经病变或Leigh综合征的患者中，核编码的线粒体异亮氨酰-tRNA合成酶IARS2发生突变。
Hum Mutat. 2014 Nov;35(11):1285-9. doi: 10.1002/humu.22629. Epub 2014 Oct 18.
5
SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors.导致多系统线粒体疾病的SDHA突变：新突变及与遗传性肿瘤的基因重叠
Eur J Hum Genet. 2015 Feb;23(2):202-9. doi: 10.1038/ejhg.2014.80. Epub 2014 Apr 30.

Does growth-hormone treatment affect patients with and without a mitochondrial disorder differentially?

作者信息

Finsterer Josef

机构信息

Krankenanstalt Rudolfstiftung, Vienna, Austria.

出版信息

Clin Pediatr Endocrinol. 2018;27(2):107-108. doi: 10.1297/cpe.27.107. Epub 2018 Apr 13.

DOI:10.1297/cpe.27.107
PMID:29662271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5897587/
Abstract
摘要