• 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

I-cell disease: clinical studies of 21 Japanese cases.

作者信息

Okada S, Owada M, Sakiyama T, Yutaka T, Ogawa M

出版信息

Clin Genet. 1985 Sep;28(3):207-15. doi: 10.1111/j.1399-0004.1985.tb00388.x.

DOI:10.1111/j.1399-0004.1985.tb00388.x
PMID:2998652
Abstract

Clinical pictures of 21 cases with I-cell disease patients, 12 males and 9 females, were analyzed. Characteristic coarse facial features and shortness of stature were observed in all cases. In general, the motor development was found to be more severely retarded than the mental development of the patients. Rather little involvement of the nervous system seemed to cause somewhat acceptable mental development in some cases, and also cause the absence of epileptic seizures in all cases. Involvement of the cardiovascular system, especially progressive hypertrophic cardiomyopathy, could be highly responsible for frequent sudden death of I-cell disease patients.

摘要

相似文献

1
I-cell disease: clinical studies of 21 Japanese cases.
Clin Genet. 1985 Sep;28(3):207-15. doi: 10.1111/j.1399-0004.1985.tb00388.x.
2
[Mucolipidosis II or "I-cell disease" in the newborn infant. 2 new cases].[新生儿黏脂贮积症II型或“I细胞病”。2例新病例]
An Esp Pediatr. 1987 Oct;27(4):297-302.
3
[Congenital epiphyseal chondrodysplasia punctata. Study of 9 cases].[先天性点状骨骺软骨发育不良。9例研究]
An Esp Pediatr. 1985 Sep;23(3):175-82.
4
First trimester prenatal evaluation for I-cell disease by N-acetyl-glucosamine 1-phosphotransferase assay.通过N-乙酰葡糖胺1-磷酸转移酶检测对I-细胞病进行孕早期产前评估。
Clin Genet. 1988 Jan;33(1):38-43. doi: 10.1111/j.1399-0004.1988.tb04262.x.
5
I-cell disease presenting with severe hypophosphatemia and cardiomyopathy.伴有严重低磷血症和心肌病的I型细胞病。
Neuropediatrics. 2000 Feb;31(1):49-50. doi: 10.1055/s-2000-15300.
6
Prenatal diagnosis of I-cell disease in the first and second trimesters.孕早期和孕中期I细胞病的产前诊断
Am J Med Sci. 1989 Jun;297(6):361-4. doi: 10.1097/00000441-198906000-00005.
7
[Mucolipidoses type II. Case report].
Rev Med Chil. 2003 Mar;131(3):314-9.
8
[The fetal alcohol syndrome. Description of 2 cases].[胎儿酒精综合征。2例病例描述]
Ann Osp Maria Vittoria Torino. 1982 Jul-Dec;25(7-12):215-25.
9
Genomic organisation of the UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) and its mutations in mucolipidosis III.UDP-N-乙酰葡糖胺-1-磷酸转移酶γ亚基(GNPTAG)的基因组结构及其在黏脂贮积症III中的突变
J Med Genet. 2004 Apr;41(4):e52. doi: 10.1136/jmg.2003.015222.
10
Mucolipidosis type II (I-cell disease) masquerading as rickets: two case reports and review of literature.伪装成佝偻病的II型黏脂贮积症(I型细胞病):两例报告并文献复习
J Pediatr Endocrinol Metab. 2012;25(1-2):191-5. doi: 10.1515/jpem-2011-0429.

引用本文的文献

1
Clinical and molecular characteristics of 20 Chinese probands with Mucolipidosis type II and III alpha/beta.20例II型和III型α/β型黏脂贮积症中国先证者的临床和分子特征
BMC Pediatr. 2024 Dec 23;24(1):830. doi: 10.1186/s12887-024-05223-x.
2
In vitro substrate reduction, chaperone and immunomodulation treatments reduce heparan sulfate in mucolipidosis III human fibroblasts.体外底物还原、伴侣蛋白和免疫调节治疗可降低黏脂贮积症III型人成纤维细胞中的硫酸乙酰肝素。
Genet Mol Biol. 2023 Dec 4;46(3 Suppl 1):e20230117. doi: 10.1590/1678-4685-GMB-2023-0117. eCollection 2023.
3
Secondary Hyperparathyroidism in Children with Mucolipidosis Type II (I-Cell Disease): Irish Experience.
II型黏脂贮积症(I-细胞病)患儿的继发性甲状旁腺功能亢进:爱尔兰的经验
J Clin Med. 2022 Mar 2;11(5):1366. doi: 10.3390/jcm11051366.
4
Hip Morphology in Mucolipidosis Type II.II型黏脂贮积症中的髋关节形态学
J Clin Med. 2020 Mar 8;9(3):728. doi: 10.3390/jcm9030728.
5
Clinical Characterization of Mucolipidoses II and III: A Multicenter Study.黏脂贮积症II型和III型的临床特征:一项多中心研究。
J Pediatr Genet. 2019 Dec;8(4):198-204. doi: 10.1055/s-0039-1697605. Epub 2019 Sep 24.
6
Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosis.韩国黏脂贮积症II/III型患者的临床、生化及分子特征分析与成功的产前诊断
Orphanet J Rare Dis. 2017 Jan 17;12(1):11. doi: 10.1186/s13023-016-0556-2.
7
Outcomes after hematopoietic stem cell transplantation for children with I-cell disease.I型细胞病患儿造血干细胞移植后的结局
Biol Blood Marrow Transplant. 2014 Nov;20(11):1847-51. doi: 10.1016/j.bbmt.2014.06.019. Epub 2014 Jul 10.
8
Mucolipidosis II: first report from Saudi Arabia.黏脂贮积症II型:沙特阿拉伯的首例报告。
Ann Saudi Med. 2013 Jul-Aug;33(4):382-6. doi: 10.5144/0256-4947.2013.382.
9
A case of mucolipidosis II presenting with prenatal skeletal dysplasia and severe secondary hyperparathyroidism at birth.一例Ⅱ型粘脂贮积症,产前出现骨骼发育异常,出生时伴有严重继发性甲状旁腺功能亢进。
Korean J Pediatr. 2012 Nov;55(11):438-44. doi: 10.3345/kjp.2012.55.11.438. Epub 2012 Nov 23.
10
Severe dilated cardiomyopathy as an unusual finding in a young infant with mucolipidosis type 2.严重扩张型心肌病是2型黏脂贮积症患儿中一种不常见的表现。
Images Paediatr Cardiol. 2006 Oct;8(4):1-6.