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
  • [21] Glycogen storage disease type III: A novel Agl knockout mouse model
    Pagliarani, Serena
    Lucchiari, Sabrina
    Ulzi, Gianna
    Violano, Raffaella
    Ripolone, Michela
    Bordoni, Andreina
    Nizzardo, Monica
    Gatti, Stefano
    Corti, Stefania
    Moggio, Maurizio
    Bresolin, Nereo
    Comi, Giacomo P.
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2014, 1842 (11): : 2318 - 2328
  • [22] Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III
    Mili, Amira
    Ben Charfeddine, Ilhem
    Mamai, Ons
    Cherif, Wafa
    Adala, Labiba
    Amara, Abdelbasset
    Pagliarani, Serena
    Lucchiari, Sabrina
    Ayadi, Abdelkarim
    Tebib, Neji
    Harbi, Abdelaziz
    Bouguila, Jihene
    H'Mida, Dorra
    Saad, Ali
    Limem, Khalifa
    Comi, G. P.
    Gribaa, Moez
    JOURNAL OF HUMAN GENETICS, 2012, 57 (03) : 170 - 175
  • [23] Skeletal and cardiac muscle involvement in children with glycogen storage disease type III
    Engy A. Mogahed
    Marian Y. Girgis
    Rodina Sobhy
    Hala Elhabashy
    Osama M. Abdelaziz
    Hanaa El-Karaksy
    European Journal of Pediatrics, 2015, 174 : 1545 - 1548
  • [24] Exercise intolerance in Glycogen Storage Disease Type III: Weakness or energy deficiency?
    Preisler, Nicolai
    Pradel, Agnes
    Husu, Edith
    Madsen, Karen Lindhardt
    Becquemin, Marie-Helene
    Mollet, Alix
    Labrune, Philippe
    Petit, Francois
    Hogrel, Jean-Yves
    Jardel, Claude
    Maillot, Francois
    Vissing, John
    Laforet, Pascal
    MOLECULAR GENETICS AND METABOLISM, 2013, 109 (01) : 14 - 20
  • [25] Liver transplantation in glycogen storage disease type III: A case-series
    Gay, Simon
    Bigot, Adrien
    d'Alteroche, Louis
    Dujardin, Fanny
    Fromont-Hankard, Gaelle
    Tressel, Nathalie
    Salame, Ephrem
    Maillot, Francois
    JIMD REPORTS, 2025, 66 (01):
  • [26] Normalization of obstructive cardiomyopathy and improvement of hepatopathy on ketogenic diet in patient with glycogen storage disease (GSD) type IIIa
    Marusic, Tatiana
    Tansek, Mojca Zerjav
    Campa, Andreja Sirca
    Mezek, Ajda
    Berden, Pavel
    Battelino, Tadej
    Groselj, Urh
    MOLECULAR GENETICS AND METABOLISM REPORTS, 2020, 24
  • [27] Skeletal and cardiac muscle involvement in children with glycogen storage disease type III
    Mogahed, Engy A.
    Girgis, Marian Y.
    Sobhy, Rodina
    Elhabashy, Hala
    Abdelaziz, Osama M.
    El-Karaksy, Hanaa
    EUROPEAN JOURNAL OF PEDIATRICS, 2015, 174 (11) : 1545 - 1548
  • [28] IMPAIRED METABOLIC FUNCTION AND SIGNALING DEFECTS IN PHAGOCYTIC-CELLS IN GLYCOGEN-STORAGE-DISEASE TYPE-1B
    KILPATRICK, L
    GARTY, BZ
    LUNDQUIST, KF
    HUNTER, K
    STANLEY, CA
    BAKER, L
    DOUGLAS, SD
    KORCHAK, HM
    JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) : 196 - 202
  • [29] Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome
    Sentner, Christiaan P.
    Hoogeveen, Irene J.
    Weinstein, David A.
    Santer, Rene
    Murphy, Elaine
    McKiernan, Patrick J.
    Steuerwald, Ulrike
    Beauchamp, Nicholas J.
    Taybert, Joanna
    Laforet, Pascal
    Petit, Francois M.
    Hubert, Aurelie
    Labrune, Philippe
    Smit, G. Peter A.
    Derks, Terry G. J.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2016, 39 (05) : 697 - 704
  • [30] Molecular diagnosis of glycogen storage disease type IX using a glycogen storage disease gene panel
    Kim, Tae Hyeong
    Kim, Kwang Yeon
    Kim, Man Jin
    Seong, Moon-Woo
    Park, Sung Sup
    Moon, Jin Soo
    Ko, Jae Sung
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2020, 63 (06)