2026-05-22T00:44:36Zhttps://repisalud.isciii.es/rest/oai/requestoai:repisalud.isciii.es:20.500.12105/140112025-03-10T15:49:04Zcom_20.500.12105_5571com_20.500.12105_2404com_20.500.12105_2403col_20.500.12105_5710
Repisalud
author
Centeno Malfaz, F
author
Bello Martínez, B
author
Beltrán Pérez, AI
author
Alcalde Martín, C
author
López García C
2022-04-18T11:22:08Z
2022-04-18T11:22:08Z
2006-10
Boletín del ECEMC: Rev Dismor Epidemiol 2006; V (nº 5): 84-90
0210–3893
Boletín del ECEMC: Revista de Dismorfología y Epidemiología
http://hdl.handle.net/20.500.12105/14011
The long QT syndrome (LQTS) is an hereditary disease that produces a malfunction on the sodium and potassium channels of the heart and lengthens the duration of the cardiac repolarization stage. It is characterized by the appearance of syncopes, arrhythmias and even sudden death. There are two variants of the congenital LQTS: the autosomal dominant Romano-Ward syndrome and the autosomal recessive Jervell-Lange-Nielsen syndrome, that is associated with sensorineural deafness and is less frequent than the other type. The diagnosis is made from the clinical criteria, the electrocardiogram and the family history. In the last few years, molecular studies have been developed, opening new possibilities not only for its diagnosis but also for the treatment of these patients.
spa
Síndrome de intervalo QT largo congénito
research article
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URL
https://repisalud.isciii.es/bitstreams/0033b873-e7de-43c5-b12d-adc981273ec1/download
File
MD5
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application/pdf
SíndromeIntervaloQTLargo_2006.pdf
URL
https://repisalud.isciii.es/bitstreams/05d871ad-ca1c-4ac3-ac69-08a37861013e/download
File
MD5
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text/plain
SíndromeIntervaloQTLargo_2006.pdf.txt