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文章 在 英语 | WPRIM | ID: wpr-80566

摘要

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.


Subject(s)
Adolescent , Humans , Male , Acidosis/etiology , Acute Disease , Barth Syndrome/diagnosis , Contrast Media/adverse effects , Frameshift Mutation , Heart Failure/etiology , Homozygote , Mutation , Pedigree , Sequence Analysis, DNA , Tomography, X-Ray Computed , Transcription Factors/genetics
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