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塞克尔综合征的色素沉着变化。

Pigmentary changes in Seckel's syndrome.

作者信息

Fathizadeh A, Soltani K, Medenica M, Lorincz A L

出版信息

J Am Acad Dermatol. 1979 Jul;1(1):52-4. doi: 10.1016/s0190-9622(79)70004-1.

DOI:10.1016/s0190-9622(79)70004-1
PMID:500866
Abstract

Seckel's syndrome consists of multiple congenital anomalies, including bird-headed dwarfism, mental deficiency, and skeletal and ophthalmic defects. We report a patient with this syndrome who demonstrated pigmentary changes, including streaks of brown pigmentation on the neck, groin, and axillae. Histologic examination revealed pigment incontinence.

摘要

塞克尔综合征由多种先天性异常组成,包括鸟头样侏儒症、智力缺陷以及骨骼和眼部缺陷。我们报告了一名患有该综合征的患者,其出现了色素沉着变化,包括颈部、腹股沟和腋窝处的褐色色素沉着条纹。组织学检查显示色素失禁。

相似文献

1
Pigmentary changes in Seckel's syndrome.塞克尔综合征的色素沉着变化。
J Am Acad Dermatol. 1979 Jul;1(1):52-4. doi: 10.1016/s0190-9622(79)70004-1.
2
[Bird headed dwarfism (Seckel's syndrome) in a girl (author's transl)].
Monatsschr Kinderheilkd (1902). 1973 Nov;121(11):689-91.
3
Seckel's syndrome: a case report.塞克尔综合征:一例病例报告。
J Med. 1993;24(1):75-96.
4
Seckel's syndrome and malformations of cortical development: report of three new cases and review of the literature.塞克尔综合征与皮质发育畸形:三例新病例报告及文献复习
J Child Neurol. 2001 May;16(5):382-6. doi: 10.1177/088307380101600516.
5
[Seckel's syndrome associated with atrial septal defect: a case report and review of the literature in Japan].[伴有房间隔缺损的塞克尔综合征:1例报告及日本文献复习]
Kyobu Geka. 1991 May;44(5):411-3.
6
[Seckel's syndrome].[塞克尔综合征]
Actas Luso Esp Neurol Psiquiatr Cienc Afines. 1980 May-Jun;8(3):211-6.
7
[Seckel's syndrome: a form of chondrodysplasia? (author's transl)].塞克尔综合征:软骨发育不良的一种形式?(作者译)
An Esp Pediatr. 1982 May;16(5):406-15.
8
Familial bird-headed dwarfism (Seckel's syndrome).
J Med Genet. 1973 Jun;10(2):196-8. doi: 10.1136/jmg.10.2.196.
9
[Seckel's syndrome (or bird's head dwarfism). Apropos of a case].[塞克尔综合征(或鸟头侏儒症)。关于一例病例]
Rev Stomatol Chir Maxillofac. 1983;84(5):264-8.
10
Bird-beaded dwarfs (Seckel's syndrome). A familial pattern of developmental, dental, skeletal, genital, and central nervous system anomalies.
J Pediatr. 1967 May;70(5):799-804. doi: 10.1016/s0022-3476(67)80334-2.

引用本文的文献

1
Central nervous system vasculopathy and Seckel syndrome: case illustration and systematic review.中枢神经系统血管病与 Seckel 综合征:病例举例与系统综述。
Childs Nerv Syst. 2021 Dec;37(12):3847-3860. doi: 10.1007/s00381-021-05284-8. Epub 2021 Aug 3.
2
A Child with Seckel Syndrome and Arterial Stenosis: Case Report and Literature Review.一名患有塞克尔综合征和动脉狭窄的儿童:病例报告及文献综述
Int Med Case Rep J. 2020 May 14;13:159-163. doi: 10.2147/IMCRJ.S241601. eCollection 2020.
3
Seckel syndrome with cutaneous pigmentary changes: two siblings and a review of the literature.
伴有皮肤色素沉着改变的塞克尔综合征:两例同胞病例及文献复习
Postepy Dermatol Alergol. 2015 Dec;32(6):470-4. doi: 10.5114/pdia.2015.56102. Epub 2015 Dec 11.
4
Intrauterine programming of ageing.衰老的宫内编程。
EMBO Rep. 2010 Jan;11(1):32-6. doi: 10.1038/embor.2009.262. Epub 2009 Dec 11.
5
A mouse model of ATR-Seckel shows embryonic replicative stress and accelerated aging.ATR-塞克尔综合征的小鼠模型表现出胚胎复制应激和加速衰老。
Nat Genet. 2009 Aug;41(8):891-8. doi: 10.1038/ng.420. Epub 2009 Jul 20.
6
Deletion of the developmentally essential gene ATR in adult mice leads to age-related phenotypes and stem cell loss.在成年小鼠中删除发育必需基因ATR会导致与年龄相关的表型和干细胞丢失。
Cell Stem Cell. 2007 Jun 7;1(1):113-126. doi: 10.1016/j.stem.2007.03.002.