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[特纳综合征女性外周血细胞计数参数的值]

[The values of peripheral blood cell count parameters in women with Turner's syndrome].

作者信息

Jez Wacław, Irzyniec Tomasz

机构信息

Slaski Uniwersytet Medyczny w Katowicach, Zakład Promocji Zdrowia i Pielegniarstwa Srodowiskowego.

出版信息

Pol Merkur Lekarski. 2010 Oct;29(172):247-9.

PMID:21207641
Abstract

UNLABELLED

Turner's syndrome is a chromosomal anomaly which occurs in approximately one in 2500 females. The syndrome is characterized by the presence of primary gonadal dysgenesia which is manifested by, among others, amenorrhoea. Taking this fact into consideration, the values of blood cell count in Turner's syndrome women could have been expected to be better than the corresponding values in the general population of women. The aim of the present research is to evaluate the basics haematology parameters in women with Turner's syndrome.

MATERIAL AND METHODS

Basic parameters of blood cell count were marked in 176 women with Turner's syndrome. One hundred and three subjects were found to have X monosomy, whereas the rest of the females had other types of karyotype. The results obtained were compared to the corresponding parameters in the general population of Polish women.

RESULTS

There were no statistically significant differences between subjects with Turner's syndrome and general female population as far as the white blood system and the red blood system parameters were concerned. Similarly, the thrombocyte count failed to be significantly different in women with Turner's syndrome and in healthy women. However, Turner's syndrome subjects with 45, X karyotype, compared to females with other karyotypes, showed a significantly higher number of thrombocytes: 267.5 +/- 70 vs 240.1 +/- 69 thousand/mm3. CONCLUSIONS. 1. Basic parameters of peripheral blood count in women with Turner's syndrome do not differ from the reference values in general female population. 2. Turner's syndrome subjects with X monosomy are characterized by a significantly higher number of thrombocytes than other women.

摘要

未标注

特纳综合征是一种染色体异常疾病,约每2500名女性中就有1例发病。该综合征的特征是原发性性腺发育不全,表现为闭经等症状。考虑到这一事实,预计特纳综合征女性的血细胞计数会优于普通女性群体的相应数值。本研究的目的是评估特纳综合征女性的基础血液学参数。

材料与方法

对176例特纳综合征女性的血细胞计数基础参数进行了记录。其中103例受试者为X单体型,其余女性具有其他类型的核型。将所得结果与波兰普通女性群体的相应参数进行比较。

结果

就白细胞系统和红细胞系统参数而言,特纳综合征患者与普通女性群体之间无统计学显著差异。同样,特纳综合征女性与健康女性的血小板计数也无显著差异。然而,与其他核型的女性相比,具有45,X核型的特纳综合征患者血小板数量显著更高:267.5±70对240.1±69千/mm³。结论。1. 特纳综合征女性外周血细胞计数的基础参数与普通女性群体的参考值无差异。2. X单体型的特纳综合征患者血小板数量显著高于其他女性。

相似文献

1
[The values of peripheral blood cell count parameters in women with Turner's syndrome].[特纳综合征女性外周血细胞计数参数的值]
Pol Merkur Lekarski. 2010 Oct;29(172):247-9.
2
Autoimmune diseases in women with Turner's syndrome.特纳综合征女性中的自身免疫性疾病。
Arthritis Rheum. 2010 Mar;62(3):658-66. doi: 10.1002/art.27270.
3
Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.促肾上腺皮质激素刺激试验和人类白细胞抗原多态性表明,特纳综合征患者及其家族中类固醇21-羟化酶缺乏症的杂合子频率较高。
Clin Endocrinol (Oxf). 1994 Jan;40(1):39-45. doi: 10.1111/j.1365-2265.1994.tb02441.x.
4
[Detection of mosaicism in women with Turner's syndrome using fluorescence in situ hybridization].[利用荧光原位杂交技术检测特纳综合征女性的嵌合体]
Cas Lek Cesk. 1999 Jun 28;138(13):396-400.
5
Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review.特纳综合征与妊娠:45,X/47,XXX嵌合体是否具有不同的预后?自身临床经验及文献综述
J Matern Fetal Neonatal Med. 2011 May;24(5):668-72. doi: 10.3109/14767058.2010.520769. Epub 2010 Oct 5.
6
Bone mineral density in Turner's syndrome and the influence of pubertal development.特纳综合征患者的骨密度与青春期发育的影响。
Acta Paediatr. 2014 Jan;103(1):e38-42. doi: 10.1111/apa.12435. Epub 2013 Nov 11.
7
Aortic distensibility and dilation in Turner's syndrome.特纳综合征中的主动脉扩张性与扩张
Cardiol Young. 2009 Dec;19(6):568-72. doi: 10.1017/S1047951109990874. Epub 2009 Oct 27.
8
The impact of obesity on cardiovascular risk factors in Turner's syndrome.肥胖对特纳综合征心血管危险因素的影响。
Clin Endocrinol (Oxf). 1998 Oct;49(4):447-50. doi: 10.1046/j.1365-2265.1998.00552.x.
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Hashimoto's disease in Turner's syndrome.特纳综合征中的桥本氏病。
Clin Invest Med. 1988 Aug;11(4):243-6.
10
[Follow-up of adult women with Turner's syndrome in a cohort study in Utrecht].[乌得勒支队列研究中成年特纳综合征女性的随访]
Ned Tijdschr Geneeskd. 2007 Jul 21;151(29):1630-4.

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1
CD4+ FOXP3+ Regulatory T Cells Exhibit Impaired Ability to Suppress Effector T Cell Proliferation in Patients with Turner Syndrome.特纳综合征患者的CD4 + FOXP3 +调节性T细胞抑制效应T细胞增殖的能力受损。
PLoS One. 2015 Dec 28;10(12):e0144549. doi: 10.1371/journal.pone.0144549. eCollection 2015.