QT-syndrome and sudden infant death

被引:0
作者
Schellscheidt, J [1 ]
Franz, C [1 ]
Loser, H [1 ]
Jorch, G [1 ]
机构
[1] Univ Munster, Klin & Poliklin Kinderheilkunde, D-48129 Munster, Germany
关键词
sudden infant death; QT-syndrome; Romano-Ward-syndrome;
D O I
10.1007/s001120050238
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Intensive epidemiologic and pathophysiologic research during the past 30 years successfully contributed to a better understanding of the etiology and pathogenesis of cot death (Sudden Infant Death, SID). However, several differential diagnoses with probable consequences for siblings should be taken into consideration,even ifa thorough postmortem examination failed to reveal an adequate cause of death. Most important are cardiac arrythmias, especially the syndrome of QT - prolongation (Romano-Ward-syndrome). The poor prognosis may be improved by prophylactic therapy with beta-blocking agents. Case: We report on two cases of prolonged QT-interval and Sudden Infant Death revealing the outstanding importance of a careful clinical observation of bereaved families, especially during subsequent pregnancies.
引用
收藏
页码:13 / 16
页数:8
相关论文
共 29 条
[1]   MOLECULAR MECHANISM FOR AN INHERITED CARDIAC-ARRHYTHMIA [J].
BENNETT, PB ;
YAZAWA, K ;
MAKITA, N ;
GEORGE, AL .
NATURE, 1995, 376 (6542) :683-685
[2]   INCIDENCE AND SIGNIFICANCE OF PRIMARY ABNORMALITIES OF CARDIAC-RHYTHM IN INFANTS AT HIGH-RISK FOR SUDDEN INFANT DEATH SYNDROME [J].
COLAN, SD ;
LIBERTHSON, RR ;
CAHEN, L ;
SHANNON, DC ;
KELLY, DH .
PEDIATRIC CARDIOLOGY, 1984, 5 (04) :267-271
[3]   A MOLECULAR-BASIS FOR CARDIAC-ARRHYTHMIA - HERG MUTATIONS CAUSE LONG QT SYNDROME [J].
CURRAN, ME ;
SPLAWSKI, I ;
TIMOTHY, KW ;
VINCENT, GM ;
GREEN, ED ;
KEATING, MT .
CELL, 1995, 80 (05) :795-803
[4]   PERMANENT CARDIAC PACING IN PATIENTS WITH THE LONG QT SYNDROME [J].
ELDAR, M ;
GRIFFIN, JC ;
ABBOTT, JA ;
BENDITT, D ;
BHANDARI, A ;
HERRE, JM ;
BENSON, DW ;
SCHEINMAN, MM .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1987, 10 (03) :600-607
[5]  
FRANEK A, 1989, MONATSSCHR KINDERH, V137, P411
[6]   THE LONG QT SYNDROME IN CHILDREN - AN INTERNATIONAL STUDY OF 287 PATIENTS [J].
GARSON, A ;
DICK, M ;
FOURNIER, A ;
GILLETTE, PC ;
HAMILTON, R ;
KUGLER, JD ;
VANHARE, GF ;
VETTER, V ;
VICK, GW .
CIRCULATION, 1993, 87 (06) :1866-1872
[7]  
GILLETTE PC, 1992, CIRCULATION, V85, P164
[8]   THE CONGENITAL LONG QT SYNDROME - AN UNUSUAL CAUSE OF CHILDHOOD SEIZURES [J].
HORN, CA ;
BEEKMAN, RH ;
DICK, M ;
LACINA, SJ .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1986, 140 (07) :659-661
[9]   CONGENITAL DEAF-MUTISM, FUNCTIONAL HEART DISEASE WITH PROLONGATION OF THE Q-T INTERVAL, AND SUDDEN DEATH [J].
JERVELL, A ;
LANGENIELSEN, F .
AMERICAN HEART JOURNAL, 1957, 54 (01) :59-68
[10]  
KAINULAINEN K, 1995, HUM GENET, V96, P395