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Inborn errors of metabolism with hyperammonemia (49-gene panel, NGS)

Code: 10175

The availability and turnaround time of this test should be confirmed with the unit before collection.

Method
Next-generation sequencing (NGS)
Collection requirements
EDTA: Blood (10 mL)
Sample stability
Refrigerated at 2-8 °C
Turnaround time
33 working days
Preparation and notes
IMPORTANT: Samples for this test should only be collected Monday to Thursday and never on the day before a public holiday. Clinical history and family history are mandatory.

Genes tested(49 genes)

  • ACADM
  • ACADS
  • ACADVL
  • ARG1
  • ASL
  • ASS1
  • BCKDHA
  • BCKDHB
  • CA5A
  • CPS1
  • CPT1A
  • CPT2
  • DBT
  • DLD
  • ETFA
  • ETFB
  • ETFDH
  • GLUD1
  • GLUL
  • HADHA
  • HADHB
  • HCFC1
  • HLCS
  • HMGCL
  • HMGCS2
  • IVD
  • MCCC1
  • MCCC2
  • MMAA
  • MMAB
  • MMACHC
  • MMADHC
  • MUT
  • NAGS
  • NBAS
  • OAT
  • OTC
  • PC
  • PCCA
  • PCCB
  • SLC22A5
  • SLC25A13
  • SLC25A15
  • SLC25A20
  • SLC7A7
  • SUCLA2
  • SUCLG1
  • TMEM70
  • UMPS

Specialties

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