• 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

Nervous system involvement in type IV glycogenosis.

作者信息

McMaster K R, Powers J M, Hennigar G R, Wohltmann H J, Farr G H

出版信息

Arch Pathol Lab Med. 1979 Mar;103(3):105-11.

PMID:284761
Abstract

A 30-month-old girl exhibited the 19th known case of type IV glycogenosis. Extensive involvement of the nervous system was found at autopsy. This represents only the second patient in whom the fine structure of the CNS and skeletal muscle has been described. We have also identified the abnormal polysaccharide in peripheral nerve, a finding that, to our knowledge, has not been reported previously. Our review of the literature indicates that approximately 50% of these patients exhibit signs or symptoms referable to the neuromuscular system. Most clinical and pathologic studies have focused on the severe liver involvement; insufficient attention has been directed toward the nervous system. This emphasizes the need for more detailed neurologic and neuropathologic examinations of children with type IV glycogenosis.

摘要

相似文献

1
Nervous system involvement in type IV glycogenosis.
Arch Pathol Lab Med. 1979 Mar;103(3):105-11.
2
Type IV glycogen storage disease: first reported case in Thailand.
J Med Assoc Thai. 1989 Dec;72(12):697-700.
3
[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)].
Arch Fr Pediatr. 1981 Dec;38 Suppl 1:837-41.
4
Juvenile polysaccharidosis with cardioskeletal myopathy.
Arch Pathol Lab Med. 1987 Oct;111(10):977-82.
5
Peripheral nerve in type III glycogenosis: selective involvement of unmyelinated fiber Schwann cells.III型糖原贮积病中的周围神经:无髓鞘纤维施万细胞的选择性受累。
Muscle Nerve. 1985 Oct;8(8):667-71. doi: 10.1002/mus.880080808.
6
Myoencephalopathies with abnormal mitochondria: a review.伴有线粒体异常的肌脑病:综述
Clin Neuropathol. 1983;2(3):101-13.
7
Neonatal type IV glycogen storage disease associated with "null" mutations in glycogen branching enzyme 1.与糖原分支酶1“无效”突变相关的新生儿IV型糖原贮积病。
J Pediatr. 2004 Nov;145(5):705-9. doi: 10.1016/j.jpeds.2004.07.024.
8
Laboratory diagnosis of the neuromuscular glycogen storage diseases.神经肌肉糖原贮积病的实验室诊断
Ann Clin Lab Sci. 1982 Nov-Dec;12(6):431-8.
9
[Recognition of glycogenosis Type IV (amylopectinosis). Ultrastructural studies in 3 brothers with juvenile liver cirrhosis].[IV型糖原贮积病(支链淀粉贮积症)的诊断。对3例青少年肝硬化兄弟的超微结构研究]
Verh Dtsch Ges Pathol. 1978;62:531.
10
Branching enzyme deficiency/glycogenosis storage disease type IV presenting as a severe congenital hypotonia: muscle biopsy and autopsy findings, biochemical and molecular genetic studies.分支酶缺陷/糖原累积症Ⅳ型表现为严重先天性肌张力低下:肌肉活检和尸检结果、生化和分子遗传学研究。
Neuromuscul Disord. 2010 Dec;20(12):783-90. doi: 10.1016/j.nmd.2010.07.275. Epub 2010 Sep 15.

引用本文的文献

1
Glycogen storage diseases: An update.糖原贮积病:更新。
World J Gastroenterol. 2023 Jul 7;29(25):3932-3963. doi: 10.3748/wjg.v29.i25.3932.
2
Case of Neonatal Fatality from Neuromuscular Variant of Glycogen Storage Disease Type IV.IV型糖原贮积病神经肌肉变异型致新生儿死亡病例
JIMD Rep. 2019;45:51-55. doi: 10.1007/8904_2018_142. Epub 2018 Oct 12.
3
Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity.患者因分支酶活性降低导致类支链淀粉物质蓄积而出现多系统受累。
J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S255-9. doi: 10.1007/s10545-008-0819-8. Epub 2008 Apr 4.
4
Glycogen storage diseases: new perspectives.糖原贮积病:新观点
World J Gastroenterol. 2007 May 14;13(18):2541-53. doi: 10.3748/wjg.v13.i18.2541.
5
[Polyglycosan body myopathy].[多糖体肌病]
Nervenarzt. 2006 Dec;77(12):1487-91. doi: 10.1007/s00115-006-2184-x.
6
Cell migration and chimerism after whole-organ transplantation: the basis of graft acceptance.全器官移植后的细胞迁移与嵌合现象:移植物接受的基础
Hepatology. 1993 Jun;17(6):1127-52.
7
Liver transplantation for type I and type IV glycogen storage disease.I型和IV型糖原贮积病的肝移植
Eur J Pediatr. 1993;152 Suppl 1(Suppl 1):S71-6. doi: 10.1007/BF02072093.
8
Uncommon types of polyglucosan bodies in the human brain: distribution and relation to disease.人脑中罕见类型的多聚葡萄糖体:分布及其与疾病的关系。
Acta Neuropathol. 1993;86(5):484-90. doi: 10.1007/BF00228584.
9
Neonatal hypotonia and cardiomyopathy secondary to type IV glycogenosis.IV型糖原贮积症继发的新生儿肌张力减退和心肌病。
Acta Neuropathol. 1994;87(5):531-6. doi: 10.1007/BF00294181.
10
Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).伴有完全性分支酶缺乏的青少年遗传性多葡聚糖体病(IV型糖原贮积病)
Acta Neuropathol. 1993;85(4):419-30. doi: 10.1007/BF00334454.