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