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Light microscopic hair shaft analysis in ectodermal dysplasia syndromes.

机译:光显微毛干分析在外胚层发育不良综合征中的应用。

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The objective of the study was to catalog hair shaft abnormalities in individuals with ectodermal dysplasia (ED) syndromes using light microscopy and to compare findings with those in unaffected controls. Light microscopy was performed in a nonblinded manner on hair shafts from 65 participants with seven types of ED (hypohidrotic ED, ED-ectrodactyly-cleft lip or palate, ankyloblepharon-ectodermal defects-cleft lip and palate, Clouston syndrome, Goltz syndrome, Schopf-Schulz Passarge syndrome, and oculodentodigital dysplasia) and 41 unaffected controls. Hair donations were collected at the 28th Annual National Family Conference held by the National Foundation for Ectodermal Dysplasia. Control participants were recruited from a private dermatology practice and an academic children's hospital outpatient dermatology clinic. Sixty-five affected participants and 41 unaffected controls were included in the analysis. We assessed the hair shafts of ED and control participants for abnormalities visible using LM. Light microscopy identified various pathologic hair shaft abnormalities in each type of ED, although none of the findings were statistically significantly different from those of the control group. Light microscopy is a poor adjuvant tool in the diagnosis of ED syndromes. Most findings are nonspecific and not sufficiently sensitive.
机译:这项研究的目的是使用光学显微镜对患有外胚层发育不良(ED)综合征的个体的发干异常进行分类,并将其发现结果与未患病对照进行比较。对来自65名参与者的7种类型的ED(低渗性ED,ED-外胚层-唇left裂,角质疏松-表皮缺损-唇left裂,Clouston综合征,Goltz综合征,Schopf-舒尔茨·帕萨尔格综合征(Schulz Passarge syndrome)和眼睑指畸形(Aculodentodigital发育不良)和41位未受影响的对照组。在国家皮肤外胚层发育不良基金会举行的第28届年度全国家庭会议上收集了捐献的头发。对照参与者是从私人皮肤科和一家儿童医院的门诊皮肤科诊所招募的。分析中包括65位受影响的参与者和41位未受影响的对照。我们评估了ED的毛干和对照组参与者使用LM可见的异常。光学显微镜检查可确定每种类型的ED的各种病理性毛干异常,尽管与对照组相比,这些发现在统计学上均无显着差异。光学显微镜是诊断ED综合征的不良辅助工具。大多数发现是非特异性的,不够敏感。

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