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[胰腺囊性纤维化中汗液的结晶形式]

[The form of crystallization of perspiration in pancreatic cystic fibrosis].

作者信息

Ferrer Calvete J, Ribes Koninckx C, Montero Brens C

机构信息

Departamento de Pediatría, Hospital Infantil La Fe, Valencia.

出版信息

An Esp Pediatr. 1990 Jun;32(6):489-91.

PMID:2221623
Abstract

The present study is based on the typical dendritic forms of the sweat crystallization from patients with cystic fibrosis (CF). The phenomenon was analyzed in sweat collected by pilocarpine iontophoresis in 26 affected subjects (Homozygotes), 42 heterozygotes and 100 healthy-control subjects. The positive crystallization pattern (dendritic form), became useful in identifying the affected patients in 100% of cases and in differentiating them from the healthy-control subjects (100%, negative crystallization). The positive crystallization pattern was not altered by decreasing the electrolytes concentration in the sweat. This test could be a help to evaluate the diagnosis of cystic fibrosis.

摘要

本研究基于囊性纤维化(CF)患者汗液结晶的典型树枝状形态。对通过毛果芸香碱离子电渗疗法收集的汗液进行了分析,涉及26名受影响受试者(纯合子)、42名杂合子和100名健康对照受试者。阳性结晶模式(树枝状形态)在100%的病例中有助于识别受影响的患者,并将他们与健康对照受试者区分开来(100%为阴性结晶)。汗液中电解质浓度降低并不会改变阳性结晶模式。该测试有助于评估囊性纤维化的诊断。

相似文献

1
[The form of crystallization of perspiration in pancreatic cystic fibrosis].[胰腺囊性纤维化中汗液的结晶形式]
An Esp Pediatr. 1990 Jun;32(6):489-91.
2
Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis.F508囊性纤维化纯合子或杂合子婴儿的汗液氯化物浓度。
Pediatrics. 1996 Apr;97(4):524-8.
3
Sweat gland bioelectrics differ in cystic fibrosis: a new concept for potential diagnosis and assessment of CFTR function in cystic fibrosis.汗腺生物电化学在囊性纤维化中存在差异:这是一个用于潜在诊断和评估囊性纤维化跨膜传导调节因子(CFTR)功能的新概念。
Thorax. 2009 Nov;64(11):932-8. doi: 10.1136/thx.2009.115295. Epub 2009 Sep 3.
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[Comparison of the classical Gibson-Cooke methods and the chloride-sensitive electrode in sweat testing for diagnosis of cystic fibrosis].[经典吉布森-库克方法与氯化物敏感电极在汗液检测诊断囊性纤维化中的比较]
Padiatr Padol. 1991;26(4):173-5.
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[Diagnosis of cystic fibrosis; simple genotyping to rule out the disease preferable to starting with the sweat test].[囊性纤维化的诊断;通过简单基因分型排除该疾病优于首先进行汗液测试]
Ned Tijdschr Geneeskd. 2003 May 24;147(21):1001-5.
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[French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening].[法国囊性纤维化新生儿筛查汗液检测操作与解读指南]
Arch Pediatr. 2010 Sep;17(9):1349-58. doi: 10.1016/j.arcped.2010.06.021. Epub 2010 Aug 16.
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Sweat testing infants detected by cystic fibrosis newborn screening.对通过囊性纤维化新生儿筛查检测出的婴儿进行汗液检测。
J Pediatr. 2005 Sep;147(3 Suppl):S69-72. doi: 10.1016/j.jpeds.2005.08.015.
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Serum CA 19-9 levels as a diagnostic marker in cystic fibrosis patients with borderline sweat tests.血清CA 19-9水平作为汗液试验临界值的囊性纤维化患者的诊断标志物。
Clin Exp Med. 2003 Sep;3(2):119-23. doi: 10.1007/s10238-003-0014-z.
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Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals.通过汗液测试诊断囊性纤维化:特定年龄的参考区间
J Pediatr. 2008 Dec;153(6):758-63. doi: 10.1016/j.jpeds.2008.04.067. Epub 2008 Jun 27.
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[Sweat testing practices in German cystic fibrosis centres].[德国囊性纤维化中心的汗液检测实践]
Klin Padiatr. 2007 Mar-Apr;219(2):70-3. doi: 10.1055/s-2007-872458.

引用本文的文献

1
Sweat chloride assay by inductively coupled plasma mass spectrometry: a confirmation test for cystic fibrosis diagnosis.采用电感耦合等离子体质谱法检测汗氯:囊性纤维化诊断的确认试验。
Anal Bioanal Chem. 2020 Oct;412(25):6909-6916. doi: 10.1007/s00216-020-02821-3. Epub 2020 Jul 21.
2
Comparison of classic sweat test and crystallization test in diagnosis of cystic fibrosis.经典汗液试验与结晶试验在囊性纤维化诊断中的比较。
Iran J Pediatr. 2012 Mar;22(1):102-6.