• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一名患有1型GM1神经节苷脂沉积症患者的色素沉着斑和斑片。

Hyperpigmented macules and patches in a patient with GM1 type 1 gangliosidosis.

作者信息

Selsor L C, Lesher J L

机构信息

Department of Dermatology, Medical College of Georgia, Augusta 30912-7400.

出版信息

J Am Acad Dermatol. 1989 May;20(5 Pt 2):878-82. doi: 10.1016/s0190-9622(89)70098-0.

DOI:10.1016/s0190-9622(89)70098-0
PMID:2497160
Abstract

We report a case of a 10-month-old male infant with GM1 type 1 gangliosidosis who also had hyperpigmented macules and patches. Light and electron microscopic findings correlated with previously published reports on findings in skin biopsy specimens of patients with lipid storage disorders. The hyperpigmented macules are most likely mongolian spots. A differential diagnosis of these lesions is discussed.

摘要

我们报告一例10个月大的男性婴儿,患有1型GM1神经节苷脂贮积症,同时伴有色素沉着的斑疹和斑片。光镜和电镜检查结果与先前发表的关于脂质贮积症患者皮肤活检标本检查结果的报告相符。色素沉着斑疹很可能是蒙古斑。本文讨论了这些病变的鉴别诊断。

相似文献

1
Hyperpigmented macules and patches in a patient with GM1 type 1 gangliosidosis.一名患有1型GM1神经节苷脂沉积症患者的色素沉着斑和斑片。
J Am Acad Dermatol. 1989 May;20(5 Pt 2):878-82. doi: 10.1016/s0190-9622(89)70098-0.
2
Report of an infant with GM1 gangliosidosis type I and extensive and unusual mongolian spots.1型GM1神经节苷脂沉积症伴广泛且异常蒙古斑婴儿的报告。
Br J Dermatol. 1981 Feb;104(2):195-200. doi: 10.1111/j.1365-2133.1981.tb00045.x.
3
Angiokeratoma corporis diffusum in GM1 gangliosidosis, type 1.
Clin Genet. 1989 Jul;36(1):59-64. doi: 10.1111/j.1399-0004.1989.tb03367.x.
4
A case of chronic GM1 gangliosidosis presenting as dystonia: clinical and biochemical studies.一例表现为肌张力障碍的慢性GM1神经节苷脂贮积症:临床与生化研究
J Neurol. 1990 Dec;237(8):491-3. doi: 10.1007/BF00314770.
5
A case of GM1 gangliosidosis type I.一例Ⅰ型GM1神经节苷脂贮积症。
Ophthalmic Paediatr Genet. 1989 Mar;10(1):63-7. doi: 10.3109/13816818909083776.
6
Infantile GM1-gangliosidosis with marked manifestation of lungs.
Acta Pathol Jpn. 1979 Mar;29(2):269-76. doi: 10.1111/j.1440-1827.1979.tb03181.x.
7
Manifestation of infantile GM1 gangliosidosis in the fetal eye. An electron microscopic study.胎儿眼部婴儿型GM1神经节苷脂贮积症的表现。一项电子显微镜研究。
Graefes Arch Clin Exp Ophthalmol. 1988;226(1):84-8. doi: 10.1007/BF02172724.
8
Adult GM1-gangliosidosis: clinical patterns and rectal biopsy.
Neurology. 1985 Jun;35(6):875-80. doi: 10.1212/wnl.35.6.875.
9
GM1 gangliosidosis presenting as neonatal ascites.
J Pediatr. 1982 Jun;100(6):940-3. doi: 10.1016/s0022-3476(82)80523-4.
10
Acquired pigmented macules in human piebald lesions. Ultrastructure of melanocytes in hypomelanotic skin.人类斑驳病病变中的后天性色素沉着斑。色素减退皮肤中黑素细胞的超微结构。
Acta Derm Venereol. 1989;69(6):524-7.

引用本文的文献

1
Clinical and Laboratory Profile of Gangliosidosis from Southern Part of India.印度南部神经节苷脂贮积症的临床和实验室特征
J Pediatr Genet. 2020 Oct 19;11(1):34-41. doi: 10.1055/s-0040-1718726. eCollection 2022 Mar.
2
Gm1 gangliosidosis associated with neonatal-onset of diffuse ecchymoses and mongolian spots.与新生儿期弥漫性瘀斑和蒙古斑相关的GM1神经节苷脂贮积症。
Indian J Dermatol. 2011 Jan;56(1):98-100. doi: 10.4103/0019-5154.77567.
3
Extensive and unusual Mongolian blue spots in a child with GM1 gangliosidosis type one.一名患有Ⅰ型GM1神经节苷脂贮积症儿童出现广泛且异常的蒙古斑。
J R Soc Med. 1992 Sep;85(9):574-5. doi: 10.1177/014107689208500922.