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Hallermann-Streiff 综合征的诊断、早期护理和治疗:文献复习。

Diagnosis, Early Care, and Treatment of Hallermann-Streiff Syndrome: A Review of the Literature.

出版信息

Pediatr Ann. 2021 May;50(5):e227-e231. doi: 10.3928/19382359-20210415-01. Epub 2021 May 1.

DOI:10.3928/19382359-20210415-01
PMID:34044702
Abstract

Hallermann-Streiff syndrome is a rare congenital disorder characterized by a wide spectrum of craniofacial abnormalities. A review of the available literature reveals that only approximately 200 cases of the disease have been reported worldwide. For this article, we performed a literature review as a basis for a proposed scheme for early care and treatment. A comprehensive database search was carried out with the use of Medline (PubMed), ISI Web of Science, and ScienceDirect/Scopus. Of the 551 studies initially found, an evaluation using inclusion and exclusion criteria ultimately resulted in a total of 33 articles. Most of the articles are case reports, and only approximately 20% of these articles include treatment options. We propose an early care and treatment schedule based on the presented symptoms. .

摘要

Hallermann-Streiff 综合征是一种罕见的先天性疾病,其特征是广泛的颅面畸形。对现有文献的回顾表明,全世界仅报道了大约 200 例该病病例。本文中,我们进行了文献回顾,为早期护理和治疗提出了一个方案。使用 Medline(PubMed)、ISI Web of Science 和 ScienceDirect/Scopus 进行了全面的数据库检索。在最初发现的 551 项研究中,通过使用纳入和排除标准进行评估,最终共有 33 篇文章被纳入。这些文章大多为病例报告,其中仅有约 20%的文章包含治疗方案。我们根据所呈现的症状提出了一个早期护理和治疗计划。

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1
Diagnosis, Early Care, and Treatment of Hallermann-Streiff Syndrome: A Review of the Literature.Hallermann-Streiff 综合征的诊断、早期护理和治疗:文献复习。
Pediatr Ann. 2021 May;50(5):e227-e231. doi: 10.3928/19382359-20210415-01. Epub 2021 May 1.
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Hallermann-Streiff syndrome with hemihypertrophy.伴有半身肥大的哈勒曼-施特雷夫综合征。
Genet Couns. 2010;21(3):329-33.
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Hallermann-Streiff syndrome: A missing molecular link for a highly recognizable syndrome.Hallermann-Streiff 综合征:一种高度可识别综合征的缺失分子联系。
Am J Med Genet C Semin Med Genet. 2018 Dec;178(4):398-406. doi: 10.1002/ajmg.c.31668.
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Hallermann-Streiff Syndrome: a case report from Turkey.
Med Oral Patol Oral Cir Bucal. 2009 May 1;14(5):E236-8.
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Cleft Palate Craniofac J. 2018 Nov;55(10):1458-1466. doi: 10.1177/1055665618765829. Epub 2018 Mar 26.
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[Spontaneous bilateral lens resorption in a case of Hallermann-Streiff syndrome].[哈勒曼-施特雷夫综合征一例的自发性双侧晶状体吸收]
Klin Monbl Augenheilkd. 1991 Sep;199(3):195-8. doi: 10.1055/s-2008-1046071.
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Atrial septal defect in Hallermann Streiff syndrome.哈利曼-施特雷夫综合征中的房间隔缺损。
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Hallermann-Streiff syndrome: clinical and psychological findings in children. Nosologic overlap with oculodentodigital dysplasia?哈勒曼-施特雷夫综合征:儿童的临床和心理学表现。与眼齿指发育不良是否存在病种重叠?
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Hallermann-Streiff syndrome: a case review.哈勒曼-施特雷夫综合征:病例回顾
Clin Exp Dermatol. 2004 Sep;29(5):477-9. doi: 10.1111/j.1365-2230.2004.01572.x.
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The early management of baby with Hallermann-Steriff-Francois Syndrome.
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Long term NIV in an infant with Hallermann-Streiff syndrome: A case report and overview of respiratory morbidity.哈勒曼-施特雷夫综合征婴儿的长期无创通气:一例报告及呼吸疾病概述
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Hallermann-Streiff syndrome diagnosed in the seventh decade of life.
在人生第七个十年诊断出的哈勒曼-施特雷夫综合征。
Am J Ophthalmol Case Rep. 2022 May 25;27:101595. doi: 10.1016/j.ajoc.2022.101595. eCollection 2022 Sep.