|
Mitocondriopatia Hepática |
Painel por Sequenciamento de Próxima Geração |
ABHD5, AGL, ATP7B, BCS1L, C10ORF2, CCDC115, CPT1A, DGUOK, GBE1, GFM1, LARS, MPV17, NBAS, PNPLA2, POLG, SCO1, SLC25A26, SUCLG1, TALDO1, TRMU, TSFM |
|
Leigh, Síndrome |
Painel por Sequenciamento de Próxima Geração |
AARS2, ACAD9, ADCK3, APTX, ATP5E, ATPAF2, BCS1L, C10ORF2, COQ2, COQ9, COX10, COX15, COX4I1, COX4I2, COX6B1, COX7A1, DARS2, DGUOK, DLAT, DLD, ETFDH, ETHE1, FASTKD2, FH, FOXRED1, GFER, GFM1, LARS2, LMBRD1, LRPPRC, MPV17, MRPS16, MTFMT, NDUFA1, NDUFA10, NDUFA11, NDUFA13, NDUFA2, NDUFA7, NDUFA8, NDUFAF1, NDUFAF2, NDUFAF3, NDUFAF4, NDUFB6, NDUFS1, NDUFS2, NDUFS3, NDUFS4, NDUFS5, NDUFS6, NDUFS7, NDUFS8, NDUFV1, NDUFV3, NUBPL, PC, PDHA1, PDHB, PDHX, PDP1, PDSS1, PDSS2, POLG, RARS2, RRM2B, SCO1, SCO2, SDHA, SDHAF1, SDHAF2, SDHB, SDHC, SDHD, SUCLA2, SUCLG1, SUCLG2, SURF1, TACO1, TK2, TMEM70, TOMM20, TRMU, TSFM, TTC19, TUFM, TUSC3, TYMP, UQCRB, UQCRQ, YARS2 |
|
Encefalopatias (Mitocondrial/Síndrome de Leigh) |
Painel por Sequenciamento de Próxima Geração |
AARS2, ACAD9, ADCK3, C10ORF2, COQ2, COQ6, COQ9, COX10, DGUOK, EARS2, ETHE1, FBXL4, MPV17, MTFMT, MTO1, NARS2, NDUFS2, NDUFS4, PDHA1, PDSS1, PDSS2, POLG, RMND1, RNASEH1, RRM2B, SCO1, SCO2, SLC19A3, SUCLA2, SUCLG1, SURF1, TK2, TMEM70, TRIT1, TRMU |
