Echocardiographic study of paediatric patients with mucopolysaccharidosis
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
15/04/2012
15/04/2012
2010
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Resumo |
Principle Mucopolysaccharidosis is an inborn error of metabolism causing glucosaminoglycans tissue storage. Cardiovascular involvement is variable but contributes significantly towards the morbidity and mortality of the patients. Objective To characterise the echocardiographic abnormalities in children and adolescents with different types of mucopolysaccharidosis. Method Echocardiograms and medical records of 28 patients aged 2–14 years, seen from 2003 to 2005, were revised. At that time, the enzymatic replacement therapy was still not available in our institution.Results Echocardiographic alterations were detected in 26 patients (93 per cent), whereas 16 (57 per cent) had abnormal auscultation, and only 6 (21 per cent) presented with cardiovascular complaint. Mitral valve thickening with dysfunction (regurgitation, stenosis, or double lesion) was diagnosed in 60.8 per cent, left ventricular hypertrophy in 43 per cent and aortic valve thickening with regurgitation in 35.8 per cent of the patients. There was no systolic dysfunction and mild left diastolic dysfunction was shown in 21.5 per cent of the patients. Pulmonary hypertension was present in 36 per cent of the patients, causing the only two deaths recorded. There was a strong association between the accumulation of dermatan sulphate and the presence of mitral valve dysfunction (p = 0.0003), aortic valve dysfunction (p = 0.006), and pulmonary hypertension (p = 0.006). Among individuals with two or more examinations, 82 per cent had a worsening evolution. Conclusions Echocardiographic alterations in children with Mucopolysaccharidosis are frequent and have a progressive character Left valve lesions, ventricular hypertrophy, and pulmonary hypertension were the most common findings and there was an association between the accumulation of dermatan sulphate and cardiovascular involvement. Unlike in adults, pulmonary hypertension was the main cause of death, not left ventricle systolic dysfunction |
Identificador |
Cardiology in the Young, Edinburgh, v. 20, n. 3, p. 254-261, 2010 1047-9511 http://producao.usp.br/handle/BDPI/14358 10.1017/S104795110999062X |
Idioma(s) |
eng |
Publicador |
Edinburgh |
Relação |
Cardiology in the Young |
Direitos |
openAccess Copyright EBSCO Industries, Inc. All rights reserved |
Palavras-Chave | #Aortic valve #Lysosomal storage diseases #Left ventricular hypertrophy #Mitral valve #Pulmonary hypertension #ERROS INATOS DO METABOLISMO DOS CARBOIDRATOS #GLICOSAMINOGLICANAS (METABOLISMO;DEFEITO) #ECOCARDIOGRAFIA (ANOMALIAS;CARACTERÍSTICAS) #HIPERTROFIA VENTRICULAR ESQUERDA #VALVA MITRAL #HIPERTENSÃO PULMONAR #LISOSSOMOS |
Tipo |
article original article publishedVersion |