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Journal of Korean Medical Science ; : 784-787, 2013.
Artículo en Inglés | WPRIM | ID: wpr-80566

RESUMEN

A 14-month-old boy was transferred because of dilated and hypertrophied left ventricle, neutropenia, and developmental delay. After checking computed tomographic angiography with contrast-dye, the patient showed acute exacerbation and finally died from multi-organ failure despite intensive cares. From genetic analysis, we revealed that the patient had Barth syndrome and found a novel hemizygous frame shift mutation in his TAZ gene, c.227delC (p.Pro76LeufsX7), which was inherited from his mother. Herein, we report a patient with Barth syndrome who had a novel mutation in TAZ gene and experienced unexpected acute exacerbation after contrast dye injection for computed tomographic angiography.


Asunto(s)
Adolescente , Humanos , Masculino , Acidosis/etiología , Enfermedad Aguda , Síndrome de Barth/diagnóstico , Medios de Contraste/efectos adversos , Mutación del Sistema de Lectura , Insuficiencia Cardíaca/etiología , Homocigoto , Mutación , Linaje , Análisis de Secuencia de ADN , Tomografía Computarizada por Rayos X , Factores de Transcripción/genética
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