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主动脉瓣狭窄与黏多糖贮积症。

Aortic stenosis and mucopolysaccharidosis.

作者信息

Wilson C S, Mankin H T, Pluth J R

出版信息

Ann Intern Med. 1980 Apr;92(4):496-8. doi: 10.7326/0003-4819-92-4-496.

DOI:10.7326/0003-4819-92-4-496
PMID:6767429
Abstract

A 43-year-old man had severe aortic stenosis and Maroteaux-Lamy syndrome (mucopolysaccharidosis, type VI). Aortic-valve replacement gave a good long-term result. Information was obtained indicating that his two brothers had also had mucopolysaccharidosis and aortic stenosis and that both had died of cardiac disease. This paper reviews the literature on cardiac involvement in mucopolysaccharidosis.

摘要

一名43岁男性患有严重主动脉瓣狭窄和马罗托-拉米综合征(黏多糖贮积症VI型)。主动脉瓣置换术取得了良好的长期效果。有信息表明,他的两个兄弟也患有黏多糖贮积症和主动脉瓣狭窄,且均死于心脏病。本文回顾了有关黏多糖贮积症心脏受累的文献。

相似文献

1
Aortic stenosis and mucopolysaccharidosis.主动脉瓣狭窄与黏多糖贮积症。
Ann Intern Med. 1980 Apr;92(4):496-8. doi: 10.7326/0003-4819-92-4-496.
2
Aortic and Mitral Valve Involvement in Maroteaux-Lamy Syndrome VI: Surgical Implications in the Enzyme Replacement Therapy Era.马罗-拉米综合征VI中的主动脉瓣和二尖瓣受累:酶替代治疗时代的手术意义
Ann Thorac Surg. 2016 Jul;102(1):e23-5. doi: 10.1016/j.athoracsur.2015.11.062.
3
Combined aortic and mitral valve replacement in an adult with mucopolysaccharidosis (Maroteaux-Lamy syndrome).一名患有黏多糖贮积症(马罗-拉米综合征)的成年人接受主动脉瓣和二尖瓣联合置换术。
Heart Vessels. 1996;11(4):215-7. doi: 10.1007/BF02559995.
4
Double valve replacement in a patient with Maroteaux - Lamy syndrome as an ultimate team challenge.马罗托-拉米综合征患者的双瓣膜置换术:终极团队挑战。
J Cardiothorac Surg. 2021 May 24;16(1):141. doi: 10.1186/s13019-021-01530-x.
5
Maroteaux-Lamy syndrome: a rare and challenging case of mitral valve replacement.马罗-拉米综合征:二尖瓣置换术的一例罕见且具有挑战性的病例。
Asian Cardiovasc Thorac Ann. 2018 Sep;26(7):560-562. doi: 10.1177/0218492316675533. Epub 2016 Oct 18.
6
Mitral stenosis in the Maroteaux-Lamy syndrome: a treatable cause of dyspnoea.马罗-拉米综合征中的二尖瓣狭窄:一种可治疗的呼吸困难病因。
Postgrad Med J. 1992 Apr;68(798):287-8. doi: 10.1136/pgmj.68.798.287.
7
Valvular heart disease in four patients with Maroteaux-Lamy syndrome.4例马罗-拉米综合征患者的心脏瓣膜病
Circulation. 1992 Jan;85(1):188-95. doi: 10.1161/01.cir.85.1.188.
8
Clearing of cornea after perforating keratoplasty in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome).
N Engl J Med. 1985 Apr 11;312(15):995. doi: 10.1056/nejm198504113121520.
9
Mental retardation in a patient with Maroteaux-Lamy.一名患有马罗-拉米综合征患者的智力发育迟缓。
Clin Genet. 1987 Feb;31(2):114-7. doi: 10.1111/j.1399-0004.1987.tb02779.x.
10
[Lamellar keratoplasty in congenital mucopolysaccharidosis of the Maroteaux-Lamy type].
Vestn Oftalmol. 1985 Nov-Dec;101(6):63-5.

引用本文的文献

1
Pre-operative Considerations in Adult Mucopolysaccharidosis Patients Planned for Cardiac Intervention.计划进行心脏介入治疗的成年黏多糖贮积症患者的术前注意事项。
Front Cardiovasc Med. 2022 Apr 4;9:851016. doi: 10.3389/fcvm.2022.851016. eCollection 2022.
2
Surgical Management of Valvular Heart Disease in Mucopolysaccharidoses: A Review of Literature.黏多糖贮积症中瓣膜性心脏病的外科治疗:文献综述
Biomedicines. 2022 Feb 4;10(2):375. doi: 10.3390/biomedicines10020375.
3
Mucopolysaccharidosis type VI: case report with first neonatal presentation with ascites fetalis and rapidly progressive cardiac manifestation.
黏多糖贮积症 VI 型:一例以胎儿腹水和快速进展性心脏表现为首发表现的新生儿病例报告。
BMC Med Genet. 2020 Feb 19;21(1):37. doi: 10.1186/s12881-020-0972-y.
4
Anesthesia in a child with Maroteaux-Lamy syndrome undergoing mitral valve replacement.患有马罗-拉米综合征的儿童在进行二尖瓣置换术时的麻醉。
Clinics (Sao Paulo). 2012;67(6):693-6. doi: 10.6061/clinics/2012(06)26.
5
Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management.黏多糖贮积症患者的心脏疾病:临床表现、诊断与治疗。
J Inherit Metab Dis. 2011 Dec;34(6):1183-97. doi: 10.1007/s10545-011-9359-8. Epub 2011 Jul 9.
6
Electrocardiographic and other cardiac anomalies in beta-glucuronidase-null mice corrected by nonablative neonatal marrow transplantation.非清髓性新生期骨髓移植纠正β-葡萄糖醛酸酶基因敲除小鼠的心电图及其他心脏异常。
Proc Natl Acad Sci U S A. 2004 Jan 13;101(2):603-8. doi: 10.1073/pnas.0305284101. Epub 2004 Jan 2.
7
Combined aortic and mitral valve replacement in an adult with mucopolysaccharidosis (Maroteaux-Lamy syndrome).一名患有黏多糖贮积症(马罗-拉米综合征)的成年人接受主动脉瓣和二尖瓣联合置换术。
Heart Vessels. 1996;11(4):215-7. doi: 10.1007/BF02559995.
8
Mucopolysaccharidosis type VI presenting in infancy with endocardial fibroelastosis and heart failure.婴儿期表现为心内膜弹力纤维增生症和心力衰竭的Ⅵ型黏多糖贮积症。
Pediatr Cardiol. 1983 Jan-Mar;4(1):61-2. doi: 10.1007/BF02281012.
9
Rare multivalvular involvement in a family of Scheie syndrome.罕见的Scheie综合征家族中的多瓣膜受累情况。
Indian J Pediatr. 1988 Mar-Apr;55(2):317-22. doi: 10.1007/BF02722209.