Author:
Stokreef Sarah,Lemos Mariana,Quintas Sofia
Abstract
We present the case of a boy in his middle childhood with gait ataxia and loss of reflexes with a 1-year onset. He had a background of an autism spectrum disorder but was otherwise healthy. A paediatric cardiology assessment was requested to investigate possible cardiac involvement associated to his neurological symptoms. Even though he had no cardiac symptoms and a normal electrocardiography, the echocardiogram revealed severe asymmetric left ventricle hypertrophy consistent with hypertrophic cardiomyopathy. This prompted genetic testing and the diagnosis of Friedreich’s ataxia was confirmed.
Reference12 articles.
1. Friedreich ataxia- pathogenesis and implications for therapies
2. National Organization of Rare Disorders. Friedreich’s ataxia, 2018. Available: https://rarediseases.org/rare-diseases/friedreichs-ataxia/
3. Consensus clinical management guidelines for Friedreich ataxia
4. Diagnosing Friedreich's ataxia;Wood;Arch Dis Child,1998
5. Gerrero-Fernadez J . Manual de Diagnóstico Y Terapéutica en Pediatría. 6th edition. Panamericana, c2017.