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Pompe's disease presenting as hypertrophic myocardiopathy with Wolff-Parkinson-White syndrome.

作者信息

Bulkley B H, Hutchins G M

出版信息

Am Heart J. 1978 Aug;96(2):246-52. doi: 10.1016/0002-8703(78)90093-5.

DOI:10.1016/0002-8703(78)90093-5
PMID:277063
Abstract
摘要

相似文献

1
Pompe's disease presenting as hypertrophic myocardiopathy with Wolff-Parkinson-White syndrome.庞贝病表现为肥厚型心肌病合并预激综合征。
Am Heart J. 1978 Aug;96(2):246-52. doi: 10.1016/0002-8703(78)90093-5.
2
[WPW syndrome combined with AV block 2 in an adult with glycogenosis (Type II)].[糖原贮积症（II型）成年患者合并预激综合征伴二度房室传导阻滞]
Wien Klin Wochenschr. 1982 Aug 6;94(15):401-4.
3
Echocardiographic evidence of outflow tract obstruction in Pompe's disease (glycogen storage disease of the heart).
Am J Cardiol. 1976 Jun;37(7):1103-6. doi: 10.1016/0002-9149(76)90433-1.
4
Cardiac arrhythmias and the adult form of type II glycogenosis.心律失常与成人型II型糖原贮积病。
N Engl J Med. 1982 Apr 15;306(15):937-8. doi: 10.1056/NEJM198204153061515.
5
De subitaneis mortibus. IX. Type A Wolff-Parkinson-White syndrome.猝死。IX. A型预激综合征。
Circulation. 1974 Dec;50(6):1264-80. doi: 10.1161/01.cir.50.6.1264.
6
[Cardiomuscular lysosomal glycogenosis in adults without known enzyme deficiency. A cause of familial myocardiopathy and lysosomal glycogen overload with normal acid maltase].
Arch Mal Coeur Vaiss. 1988 Jan;81(1):109-14.
7
Generalized glycogenosis type II (Pompe's disease).II型糖原贮积症（庞贝氏病）。
Arch Dis Child. 1970 Feb;45(239):122-9. doi: 10.1136/adc.45.239.122.
8
[Familial hypertrophic cardiomyopathy associated with Wolff-Parkinson-White syndrome revealing type II glycogenosis].
Arch Pediatr. 2002 Jul;9(7):697-700. doi: 10.1016/s0929-693x(01)00968-x.
9
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.过表达突变型PRKAG2的转基因小鼠确定了糖原贮积性心肌病中预激综合征的病因。
Circulation. 2003 Jun 10;107(22):2850-6. doi: 10.1161/01.CIR.0000075270.13497.2B. Epub 2003 Jun 2.
10
An interesting case of infant sudden death: severe hypertrophic cardiomyopathy in Pompe's disease.
Pacing Clin Electrophysiol. 1999 May;22(5):821-2. doi: 10.1111/j.1540-8159.1999.tb00551.x.

引用本文的文献

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Hypertrophic Cardiomyopathy and Ventricular Preexcitation in the Young: Cause and Accessory Pathway Characteristics.肥厚型心肌病和年轻人的心室预激：病因和旁路特征。
Circ Arrhythm Electrophysiol. 2023 Nov;16(11):e012191. doi: 10.1161/CIRCEP.123.012191. Epub 2023 Oct 25.
2
A Comprehensive Update on Late-Onset Pompe Disease.晚期庞贝病的全面更新。
Biomolecules. 2023 Aug 22;13(9):1279. doi: 10.3390/biom13091279.
3
Clinical and biochemical footprints of inherited metabolic diseases. IV. Metabolic cardiovascular disease.
遗传性代谢疾病的临床和生化特征。四、代谢性心血管疾病。
Mol Genet Metab. 2021 Feb;132(2):112-118. doi: 10.1016/j.ymgme.2020.12.290. Epub 2020 Dec 25.
4
Right ventricular function in late-onset Pompe disease.迟发性庞贝病患者的右心室功能。
J Clin Monit Comput. 2014 Aug;28(4):419-21. doi: 10.1007/s10877-014-9551-0. Epub 2014 Jan 14.
5
Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy.迟发性庞贝病的心血管异常和酶替代治疗反应。
Genet Med. 2011 Jul;13(7):625-31. doi: 10.1097/GIM.0b013e3182142966.
6
Combined general and epidural anesthesia for major abdominal surgery in a patient with Pompe disease.庞贝病患者行大腹部手术的全身麻醉与硬膜外麻醉联合应用。
J Anesth. 2010 Oct;24(5):768-73. doi: 10.1007/s00540-010-0984-4. Epub 2010 Jul 9.
7
The frequency and functional impact of overlapping hypertension on hypertrophic cardiomyopathy: a single-center experience.高血压重叠对肥厚型心肌病的发生频率和功能影响：单中心经验。
J Clin Hypertens (Greenwich). 2010 Apr;12(4):240-5. doi: 10.1111/j.1751-7176.2009.00251.x.
8
Lysosomal storage disorders in the newborn.新生儿溶酶体贮积症
Pediatrics. 2009 Apr;123(4):1191-207. doi: 10.1542/peds.2008-0635.
9
Arrhythmias in patients receiving enzyme replacement therapy for infantile Pompe disease.接受婴儿型庞贝病酶替代疗法患者的心律失常
Genet Med. 2008 Oct;10(10):758-62. doi: 10.1097/GIM.0b013e318183722f.
10
Reversibility of PRKAG2 glycogen-storage cardiomyopathy and electrophysiological manifestations.PRKAG2糖原贮积性心肌病及电生理表现的可逆性
Circulation. 2008 Jan 15;117(2):144-54. doi: 10.1161/CIRCULATIONAHA.107.726752. Epub 2007 Dec 24.