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J Pediatr ; 193: 256-260, 2018 02.
Article in English | MEDLINE | ID: mdl-29249525

ABSTRACT

The diagnosis of Barth syndrome is challenging owing to the wide phenotypic spectrum with allelic heterogeneity. Here we report 3 cases of Barth syndrome with phenotypic and allelic heterogeneity that were diagnosed by different approaches, including whole exome sequencing and final confirmation by reverse-transcription polymease chain reaction.


Subject(s)
Barth Syndrome/diagnosis , Transcription Factors/genetics , Acyltransferases , Barth Syndrome/genetics , Humans , Infant , Infant, Newborn , Male , Mutation , Phenotype , Reverse Transcriptase Polymerase Chain Reaction/methods , Exome Sequencing/methods
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