• 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

相似文献

1
Carbonic anhydrase II deficiency: report of a novel mutation.碳酸酐酶 II 缺乏症:一种新突变的报告。
CEN Case Rep. 2016 May;5(1):108-112. doi: 10.1007/s13730-015-0205-y. Epub 2015 Dec 8.
2
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosis.碳酸酐酶II缺乏的拟表型:伴有远端肾小管酸中毒的遗传性婴儿骨硬化症的一种新的遗传学解释。
J Med Genet. 2003 Feb;40(2):115-21. doi: 10.1136/jmg.40.2.115.
3
Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal tubular acidosis and brain calcification): novel mutations in CA2 identified by direct sequencing expand the opportunity for genotype-phenotype correlation.碳酸酐酶II缺乏综合征(伴有肾小管酸中毒和脑钙化的骨质石化症):通过直接测序鉴定出的CA2新突变增加了基因型与表型相关性研究的机会。
Hum Mutat. 2004 Sep;24(3):272. doi: 10.1002/humu.9266.
4
Carbonic anhydrase II deficiency.碳酸酐酶 II 缺乏症。
Bone. 2023 Apr;169:116684. doi: 10.1016/j.bone.2023.116684. Epub 2023 Jan 27.
5
Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.12个患有常染色体隐性遗传的骨硬化症伴肾小管酸中毒和脑钙化综合征家庭中的碳酸酐酶II缺乏症
N Engl J Med. 1985 Jul 18;313(3):139-45. doi: 10.1056/NEJM198507183130302.
6
Paralysis Episodes in Carbonic Anhydrase II Deficiency.
Saudi J Kidney Dis Transpl. 2003 Jan-Mar;14(1):70-4.
7
The neurology of carbonic anhydrase type II deficiency syndrome.碳酸酐酶缺乏症Ⅱ型的神经学表现。
Brain. 2011 Dec;134(Pt 12):3502-15. doi: 10.1093/brain/awr302. Epub 2011 Nov 26.
8
Evaluation of carbonic anhydrase isozymes in disorders involving osteopetrosis and/or renal tubular acidosis.在涉及骨质石化症和/或肾小管酸中毒的病症中对碳酸酐酶同工酶的评估。
Clin Biochem. 1991 Aug;24(4):311-8. doi: 10.1016/0009-9120(91)80005-n.
9
Report of Another Mutation Proven Case of Carbonic Anhydrase II Deficiency.另一例经证实的碳酸酐酶II缺乏症突变病例报告。
J Pediatr Genet. 2019 Jun;8(2):91-94. doi: 10.1055/s-0038-1675781. Epub 2018 Nov 18.
10
Carbonic anhydrase II deficiency syndrome: recessive osteopetrosis with renal tubular acidosis and cerebral calcification.碳酸酐酶 II 缺乏综合征:伴有肾小管酸中毒和脑钙化的隐性骨硬化症。
Pediatrics. 1986 Mar;77(3):371-81.

引用本文的文献

1
Carbonic Anhydrase II Deficiency: Unusual Presentation of the Arabic Mutation. A Case Report.碳酸酐酶II缺乏症:阿拉伯突变的罕见表现。病例报告。
Glob Pediatr Health. 2024 Feb 7;11:2333794X241230873. doi: 10.1177/2333794X241230873. eCollection 2024.
2
regulates osteoclastogenesis by inhibiting the c‑Fos/NFATc1 pathway and alleviating bone loss in an ovariectomy model.通过抑制 c-Fos/NFATc1 通路调节破骨细胞生成,并在卵巢切除模型中缓解骨质流失。
Mol Med Rep. 2023 Oct;28(4). doi: 10.3892/mmr.2023.13074. Epub 2023 Aug 18.
3
Blessing in disguise: when head trauma solves the riddle of carbonic anhydrase II deficiency.因祸得福:头部外伤解开碳酸酐酶II缺乏之谜时
Radiol Case Rep. 2022 Jan 6;17(3):847-851. doi: 10.1016/j.radcr.2021.12.004. eCollection 2022 Mar.
4
Report of Another Mutation Proven Case of Carbonic Anhydrase II Deficiency.另一例经证实的碳酸酐酶II缺乏症突变病例报告。
J Pediatr Genet. 2019 Jun;8(2):91-94. doi: 10.1055/s-0038-1675781. Epub 2018 Nov 18.
5
One Disease, Many Genes: Implications for the Treatment of Osteopetroses.一种疾病,多个基因:对骨硬化症治疗的启示
Front Endocrinol (Lausanne). 2019 Feb 19;10:85. doi: 10.3389/fendo.2019.00085. eCollection 2019.
6
Genetics of Osteopetrosis.成骨不全症的遗传学。
Curr Osteoporos Rep. 2018 Feb;16(1):13-25. doi: 10.1007/s11914-018-0415-2.

本文引用的文献

1
Allelic heterogeneity in inbred populations: the Saudi experience with Alström syndrome as an illustrative example.近交群体中的等位基因异质性:以沙特阿拉伯阿尔斯特伦综合征的经验为例
Am J Med Genet A. 2009 Feb 15;149A(4):662-5. doi: 10.1002/ajmg.a.32753.
2
Paralysis Episodes in Carbonic Anhydrase II Deficiency.
Saudi J Kidney Dis Transpl. 2003 Jan-Mar;14(1):70-4.
3
Long-term follow up of carbonic anhydrase II deficiency syndrome.
Saudi Med J. 2002 Jan;23(1):25-9.
4
Bone marrow transplantation corrects osteopetrosis in the carbonic anhydrase II deficiency syndrome.骨髓移植可纠正碳酸酐酶 II 缺乏综合征中的骨质石化症。
Blood. 2001 Apr 1;97(7):1947-50. doi: 10.1182/blood.v97.7.1947.
5
Hearing impairment in association with distal renal tubular acidosis among Saudi children.沙特儿童中听力障碍与远端肾小管酸中毒的关联
J Laryngol Otol. 1995 Oct;109(10):930-4. doi: 10.1017/s0022215100131706.
6
Marble brain disease: recessive osteopetrosis, renal tubular acidosis and cerebral calcification in three Saudi Arabian families.大理石脑疾病:三个沙特阿拉伯家庭中的隐性骨硬化症、肾小管性酸中毒和脑钙化
Dev Med Child Neurol. 1980 Feb;22(1):72-84. doi: 10.1111/j.1469-8749.1980.tb04307.x.
7
Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8.人类碳酸酐酶II的多态性基因:一个位于8号染色体上的分子疾病标志物。
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4437-40. doi: 10.1073/pnas.80.14.4437.
8
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.碳酸酐酶II缺乏被确定为伴有肾小管酸中毒和脑钙化的常染色体隐性骨硬化综合征的主要缺陷。
Proc Natl Acad Sci U S A. 1983 May;80(9):2752-6. doi: 10.1073/pnas.80.9.2752.
9
Osteopetrosis associated with proximal and distal tubular acidosis.
Acta Paediatr Scand. 1972 Jul;61(4):429-34. doi: 10.1111/j.1651-2227.1972.tb15859.x.
10
[Osteopetrosis and renal tubular acidosis. 2 cases of this association in a sibship].[骨硬化症与肾小管酸中毒。一个家族中出现这种关联的2例病例]
Arch Fr Pediatr. 1972 Mar;29(3):269-86.

碳酸酐酶 II 缺乏症:一种新突变的报告。

Carbonic anhydrase II deficiency: report of a novel mutation.

作者信息

Alsharidi Aynaa, Al-Hamed Mohammad, Alsuwaida Abdulkareem

机构信息

Department of Medicine (38), College of Medicine, King Saud University, P.O. Box 2925, Riyadh, 11461, Kingdom of Saudi Arabia.

Department of Genetics, King Faisal Specialist and Research Center, Riyadh, Kingdom of Saudi Arabia.

出版信息

CEN Case Rep. 2016 May;5(1):108-112. doi: 10.1007/s13730-015-0205-y. Epub 2015 Dec 8.

DOI:10.1007/s13730-015-0205-y
PMID:28509178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5411668/
Abstract

Carbonic anhydrase II (CAII) deficiency is an autosomal recessive disorder characterized by renal tubular acidosis, osteopetrosis, recurrent bone fractures, renal stones, growth failure, and mental retardation. Several cases have been reported in Saudi Arabia with homozygous mutations in CA2 consistent with a high degree of consanguinity. We report a case of carbonic anhydrase II deficiency with short stature, mixed renal tubular acidosis, recurrent bone fractures due to trivial trauma, recurrent renal stones and cerebral calcification. This patient was compound heterozygous for a novel CA2 mutation and a previously reported mutation in Arabs.

摘要

碳酸酐酶II(CAII)缺乏症是一种常染色体隐性疾病,其特征为肾小管酸中毒、骨硬化、反复骨折、肾结石、生长发育迟缓及智力障碍。沙特阿拉伯已报道多例CA2基因纯合突变病例,这与高度近亲结婚有关。我们报告1例碳酸酐酶II缺乏症患者,该患者身材矮小,患有混合型肾小管酸中毒,因轻微外伤反复骨折,反复发生肾结石及脑钙化。该患者为一种新的CA2突变与先前报道的阿拉伯人群突变的复合杂合子。