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J Pediatr ; 189: 222-226.e1, 2017 10.
Article in English | MEDLINE | ID: mdl-28947054

ABSTRACT

We present cases of 3 children diagnosed with the same genetic condition, Gitelman syndrome, at different stages using various genetic methods: panel testing, targeted single gene sequencing, and exome sequencing. We discuss the advantages and disadvantages of each method and review the potential of genomic sequencing for early disease detection.


Subject(s)
Genetic Diseases, Inborn/diagnosis , Gitelman Syndrome/diagnosis , Sequence Analysis, DNA/methods , Adolescent , Child , Child, Preschool , Early Diagnosis , Genetic Testing/methods , Humans , Male
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