Abstract

OBJECTIVES:The present study aims to describe the clinical, electrocardiographic, and echocardiographic cardiological findings in a group of patients with oral clefts.METHODS:This is a prospective cross-sectional study on 70 children (age range from 13 days to 19 years) with oral clefts who attended the multidisciplinary program of a university hospital from March 2013 to September 2014. The patients were evaluated by a pediatric cardiologist and underwent detailed anamnesis, physical examination, electrocardiogram, and echocardiogram.RESULTS:Sixty percent of the patients were male; 55.7% presented with cleft lip and palate, and 40.0% presented with health complaints. Comorbidities were found in 44.3%. Relevant pregnancy, neonatal, family and personal antecedents were present in 55.7%, 27.1%, 67.2%, and 24.3% of the patients, respectively. Regarding the antecedents, 15.2% of the patients presented with a cardiac murmur, 49.0% with a familial risk of developing plurimetabolic syndrome, and 6% with family antecedents of rheumatic fever. Electrocardiographic evaluation showed one case of atrioventricular block. Echocardiograms were abnormal in 35.7% of the exams, including 5 cases of mitral valve prolapse — one of which was diagnosed with rheumatic heart disease.CONCLUSION:The finding of a family risk of developing plurimetabolic syndrome and a diagnosis of rheumatic heart disease indicates that patients with oral clefts may be more prone to developing acquired heart disease. Thus, our findings highlight the importance of anamnesis and methodological triangulation (clinical-electrocardiographic-echocardiographic) in the investigation of patients with oral clefts and emphasize that cardiological follow-up to evaluate acquired and/or rhythm heart diseases is necessary. This strategy permits comorbidity prevention and individualized planned treatment.

Highlights

  • Oral clefts (OCs) are a heterogeneous group of important congenital defects with a prevalence of 1:500-1000 live births [1,2]

  • Regarding OC type, 40 (55.1%) patients presented with cleft lip and palate (CLP), and familial cleft history was noted in 32.9% of patients

  • A pediatrician evaluated all patients, and most had undergone some type of OC correction

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Summary

Introduction

Oral clefts (OCs) are a heterogeneous group of important congenital defects with a prevalence of 1:500-1000 live births [1,2]. OCs are recognized by the World Health Organization (WHO) as a public health problem [3]. In 70% of cases, OCs have an isolated presentation (non-syndromic), whereas the rest are associated with other congenital defects (syndromic) [1,2]. No potential conflict of interest was reported. Received for publication on May 9, 2017.

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