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GTR Home > Tests > Galactose epimerase deficiency, 230350, Autosomal recessive (Galactosemia) (GALE gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Overview

Test order codeHelp: 6288

Test name

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Galactose epimerase deficiency, 230350, Autosomal recessive (Galactosemia) (GALE gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Purpose of the test

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This is a clinical test intended for Help: Diagnosis

Condition

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How to order

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Not provided

Methodology

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Molecular Genetics
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

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Clinical utility

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Not provided

Clinical validity

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Not provided

Practice guidelines

  • ACMG Algorithm, 2022
    American College of Medical Genetics Algorithm, Primary or Secondary Hypergalactosemia (Galactose Elevated)
  • ACMG ACT, 2022
    American College of Medical Genetics and Genomics, Newborn Screening ACT Sheet, Elevated total galactose with normal GALT enzyme activity, Primary or Secondary Hypergalactosemia, 2022
  • ACMG ACT, 2022
    American College of Medical Genetics ACT Sheet, Newborn Screening ACT Sheet Primary or Secondary Hypergalactosemia
  • ACMG ACT Sheet, 2010
    American College of Medical Genetics ACT SHEETs, Primary or Secondary Hypergalactosemia, 2010
  • ACMG Algorithm, 2009
    American College of Medical Genetics Algorithm, Primary or Secondary Hypergalactosemia, 2009

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