Clinical and biochemical spectrum of metabolic cardiomyopathy in Egyptian children

Background: Inborn errors of metabolism (IEMs) commonly present with pediatric cardiomyopathy. Identification of the underlying cause is necessary as it may lead to improved outcomes. Objectives: We aimed to investigate the diagnostic rate, the clinical, and biochemical spectra of IEMs among Egyptia...

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Main Authors: Almenabawy, N.M (Author), Ammar, R.I (Author), Elmonem, M.A (Author), El-Saiedi, S.A (Author), Ismail, R.I (Author), Mehaney, D.A (Author), Saad, I.A.E (Author), Seliem, Z.S (Author), Selim, L.A.E (Author), Soliman, M.M (Author)
Format: Article
Language:English
Published: Makerere University, Medical School 2022
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Online Access:View Fulltext in Publisher
LEADER 02457nam a2200277Ia 4500
001 10.4314-ahs.v22i1.26
008 220630s2022 CNT 000 0 und d
020 |a 16806905 (ISSN) 
245 1 0 |a Clinical and biochemical spectrum of metabolic cardiomyopathy in Egyptian children 
260 0 |b Makerere University, Medical School  |c 2022 
520 3 |a Background: Inborn errors of metabolism (IEMs) commonly present with pediatric cardiomyopathy. Identification of the underlying cause is necessary as it may lead to improved outcomes. Objectives: We aimed to investigate the diagnostic rate, the clinical, and biochemical spectra of IEMs among Egyptian pediatric patients presenting with cardiomyopathy, and their outcome measures. Methods: We retrospectively analyzed the clinical, biochemical, and radiological data of 1512 children diagnosed with cardiomyopathy at Cairo University Children’s Hospital over a 5-year duration. Results: Two hundred twenty-nine children were clinically suspected as IEMs and underwent metabolic workup. Nineteen different IEMs were confirmed in 57 (24.4%) of the suspected children. Their median age at presentation was 2.6 years and the majority had extra-cardiac manifestations. Hypertrophic cardiomyopathy represented 43/57 (75.4%) of confirmed cases, while dilated cardiomyopathy represented 13/57 (22.8%), and one patient presented with a mixed phenotype. Twenty- six patients (45.6%) survived, while 31 patients (54%) either died or were lost to follow up and assumed deceased. Conclusions: We developed for the first time a database and a diagnostic scheme for metabolic cardiomyopathies in Egyptian children. With the recent introduction of enzyme replacement therapy, many metabolic disorders became treatable, thus establishing an early and accurate diagnosis is extremely important. © 2022 Seliem ZS et al. Licensee African Health Sciences. 
650 0 4 |a Cardiomyopathy 
650 0 4 |a Inborn errors of metabolism 
650 0 4 |a Pediatric 
700 1 0 |a Almenabawy, N.M.  |e author 
700 1 0 |a Ammar, R.I.  |e author 
700 1 0 |a Elmonem, M.A.  |e author 
700 1 0 |a El-Saiedi, S.A.  |e author 
700 1 0 |a Ismail, R.I.  |e author 
700 1 0 |a Mehaney, D.A.  |e author 
700 1 0 |a Saad, I.A.E.  |e author 
700 1 0 |a Seliem, Z.S.  |e author 
700 1 0 |a Selim, L.A.E.  |e author 
700 1 0 |a Soliman, M.M.  |e author 
773 |t African Health Sciences 
856 |z View Fulltext in Publisher  |u https://doi.org/10.4314/ahs.v22i1.26