Cardiac Abnormalities in Congenital and Childhood Myotonic Muscular Dystrophy Type 1

被引:8
|
作者
Sharma, Anjali [1 ]
Singh, Sandeep [2 ]
Mishra, Shri K. [3 ,4 ,5 ]
机构
[1] Univ Southern Calif, Keck Sch Med, Los Angeles, CA USA
[2] Western Univ Hlth & Sci, Coll Osteopath Med Pacific, Pomona, CA USA
[3] Univ Southern Calif, Keck Sch Med, Dept Neurol, Los Angeles, CA USA
[4] UCLA, David Geffen Sch Med, Los Angeles, CA USA
[5] Olive View Med Ctr, Dept Neurol, Sylmar, CA USA
关键词
congenital myotonic dystrophy type 1; cardiac abnormalities; myotonic dystrophy type 1; DM1; childhood DM1;
D O I
10.1055/s-0036-1597546
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Myotonic dystrophy often presents with cardiac abnormalities, particularly conduction defects, that factor into an increased risk of sudden cardiac death. Myotonic dystrophy has two forms, myotonic dystrophy type 1 (DM1) and DM2, and is a multisystemic disorder that presents in a wide, clinical spectrum and age range. A distinguishing feature of DM1 is the existence of a congenital form. Though research on cardiac involvement has been conducted on patients with the adult form of myotonic dystrophy, there have been few studies focused on cardiac involvement in pediatric patients with congenital myotonic dystrophy type 1 (CDM1). In this study, a survey was conducted to determine the prevalence and variations of cardiac abnormalities in pediatric patients with CDM1. This preliminary study found a prevalence of 25.8% CDM1 pediatric patients with cardiac abnormalities in a sample size of 31 patients.
引用
收藏
页码:42 / 44
页数:3
相关论文
共 50 条
  • [31] Electrocardiographic abnormalities and sudden death in myotonic dystrophy type 1
    Estes, N. A. Mark, III
    HEART RHYTHM, 2008, 5 (09) : 1358 - 1358
  • [32] SUDDEN CARDIAC DEATH IN MYOTONIC DYSTROPHY TYPE 1
    Hanson, Emily
    Walther, Stewart
    Raizada, Veena
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2018, 71 (11) : 2412 - 2412
  • [33] Noncompaction in myotonic dystrophy type 1 on cardiac MRI
    Finsterer, J
    Stöllberger, C
    Kopsa, W
    CARDIOLOGY, 2005, 103 (03) : 167 - 168
  • [34] Cardiac involvement in Fukuyama-type congenital muscular dystrophy
    Nakanishi, Toshio
    Sakauchi, Masako
    Kaneda, Yoshio
    Tomimatsu, Hirofumi
    Saito, Kayoko
    Nakazawa, Makoto
    Osawa, Makiko
    PEDIATRICS, 2006, 117 (06) : E1187 - E1192
  • [35] ANAL ABNORMALITIES IN CHILDHOOD MYOTONIC-DYSTROPHY - COMMENT
    REARDON
    HUGHES
    GREEN
    HARPER
    ARCHIVES OF DISEASE IN CHILDHOOD, 1992, 67 (11) : 1412 - 1412
  • [36] CARDIAC INVOLVEMENT IN CONGENITAL MYOTONIC-DYSTROPHY
    FORSBERG, H
    OLOFSSON, BO
    ERIKSSON, A
    ANDERSSON, S
    BRITISH HEART JOURNAL, 1990, 63 (02): : 119 - 121
  • [37] Difference of the mechanism of dysphagia between Duchenne muscular dystrophy and myotonic dystrophy type 1
    Furuya, H.
    Umemoto, G.
    Kikuta, T.
    Arahata, H.
    Fujii, N.
    NEUROMUSCULAR DISORDERS, 2013, 23 (9-10) : 792 - 792
  • [38] Association of spinal and bulbar muscular atrophy with myotonic dystrophy type 1
    Jinnai, K
    Nishimoto, K
    Itoh, K
    Hashimoto, K
    Takahashi, K
    MUSCLE & NERVE, 2004, 29 (05) : 729 - 733
  • [39] Muscular fat fraction correlates with functionality in myotonic dystrophy type 1
    Heskamp, L.
    van Nimwegen, M.
    Bassez, G.
    Jimenez-Moreno, A.
    Ploegmakers, M.
    Deux, J.
    Gorman, G.
    Lochmuller, H.
    Catt, M.
    van Engelen, B.
    Heerschap, A.
    NEUROMUSCULAR DISORDERS, 2017, 27 : S180 - S180
  • [40] Cognition and adaptive skills in myotonic dystrophy type 1: a study of 55 individuals with congenital and childhood forms
    Ekstrom, Anne-Berit
    Hakenas-Plate, Louise
    Tulinius, Mar
    Wentz, Elisabet
    DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2009, 51 (12): : 982 - 990