CARDIOMYOPATHY OF GLYCOGEN-STORAGE-DISEASE TYPE-III

被引:20
|
作者
CARVALHO, JS
MATTHEWS, EE
LEONARD, JV
DEANFIELD, J
机构
[1] Department of Paediatric Cardiology, Hospitals for Sick Children, London, WC1N 3JH, Great Ormond Street
[2] Institute of Child Health, London, WC1N 1EH
关键词
CARDIOMYOPATHY; GLYCOGEN STORAGE DISEASE; ECHOCARDIOGRAPHY;
D O I
10.1007/BF01744800
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To identify the severity of cardiac involvement in glycogen storage disease type III (GSDIII), and its relation to skeletal muscle involvement and age, 23 patients were studied. The median age was 10 years. Echocardiography, electrocardiography, and creatine phosphokinase (CK) levels were used to assess cardiac and skeletal muscle involvement. Septal and left ventricular posterior wall measurements were compared with normal data. Shortening fraction was derived from left ventricular cavity dimensions. In some patients the echocardiogram resembled that of hypertrophic cardiomyopathy. Thirteen of 20 electrocardiograms (ECG) were abnormal. Eleven patients had septal and/or posterior wall thickness >95% confidence limits (CL). Despite this, cardiac symptoms were uncommon. The CK levels were not directly associated with cardiac abnormalities. Older patients (>20 years) had more abnormal measurements of posterior wall thickness than did younger ones (<20 years). This finding, albeit in a cross-sectional series, suggests progressive myocardial involvement with age despite the absence of symptoms.
引用
收藏
页码:155 / 159
页数:5
相关论文
共 50 条
  • [31] GLYCOGEN-STORAGE-DISEASE IN CATS
    FYFE, JC
    JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 1995, 206 (03) : 286 - 287
  • [32] GLYCOGEN-STORAGE-DISEASE TYPE-I - REPLY
    SCHWENK, WF
    HAYMOND, MW
    NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (08): : 521 - 521
  • [33] DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE
    SHIN, YS
    JOURNAL OF INHERITED METABOLIC DISEASE, 1990, 13 (04) : 419 - 434
  • [34] GLYCOGEN-STORAGE-DISEASE IN ADULTS
    TALENTE, GM
    COLEMAN, RA
    ALTER, C
    BAKER, L
    BROWN, BI
    CANNON, RA
    CHEN, YT
    CRIGLER, JF
    FERREIRA, P
    HAWORTH, JC
    HERMAN, GE
    ISSENMAN, RM
    KEATING, JP
    LINDE, R
    ROE, TF
    SENIOR, B
    WOLFSDORF, JI
    ANNALS OF INTERNAL MEDICINE, 1994, 120 (03) : 218 - 226
  • [35] HEPATIC GLYCOGEN-STORAGE-DISEASE
    COLLINS, JE
    LEONARD, JV
    BRITISH JOURNAL OF HOSPITAL MEDICINE, 1987, 38 (03) : 168 - +
  • [36] Plasma creatine kinase and cardiomyopathy in glycogen storage disease type III
    Lee, P
    Burch, M
    Leonard, JV
    JOURNAL OF INHERITED METABOLIC DISEASE, 1995, 18 (06) : 751 - 752
  • [37] Obstructive hypertrophic cardiomyopathy in type III glycogen-storage disease
    Cuspidi, C
    Sampieri, L
    Pelizzoli, S
    Pontiggia, G
    Zanchetti, A
    Nappo, A
    Caputo, V
    Matturri, L
    ACTA CARDIOLOGICA, 1997, 52 (02) : 117 - 123
  • [38] The incidence and natural course of cardiomyopathy in Glycogen Storage Disease type III
    Sentner, Christiaan P.
    Smit, G. Peter A.
    MOLECULAR GENETICS AND METABOLISM, 2012, 105 (03) : 295 - 295
  • [39] BONE MINERALIZATION IN TYPE-1 GLYCOGEN-STORAGE-DISEASE
    LEE, PJ
    PATEL, JS
    FEWTRELL, M
    LEONARD, JV
    BISHOP, NJ
    EUROPEAN JOURNAL OF PEDIATRICS, 1995, 154 (06) : 483 - 487
  • [40] RENAL COMPLICATIONS IN GLYCOGEN-STORAGE-DISEASE TYPE-I
    REITSMABIERENS, WCC
    EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 : S60 - S62