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Journal of Korean Medical Science ; : 784-787, 2013.
Artigo em Inglês | WPRIM | ID: wpr-80566

RESUMO

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.


Assuntos
Adolescente , Humanos , Masculino , Acidose/etiologia , Doença Aguda , Síndrome de Barth/diagnóstico , Meios de Contraste/efeitos adversos , Mutação da Fase de Leitura , Insuficiência Cardíaca/etiologia , Homozigoto , Mutação , Linhagem , Análise de Sequência de DNA , Tomografia Computadorizada por Raios X , Fatores de Transcrição/genética
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