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Piruvato Desidrogenase, Deficiência |
Sequenciamento Completo do Gene |
PDHA1 |
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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 |
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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 |
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Distonia, Discinesia |
Painel por Sequenciamento de Próxima Geração |
ACY1, ADCY5, ANO3, ATM, ATP13A2, ATP1A3, CACNA1B, CIZ1, COL6A3, DLAT, GCDH, GCH1, GNAL, HPCA, KCNMA1, KCTD17, MR1, PDHA1, PDHX, PLA2G6, PNKD, PRKRA, PRRT2, RELN, SCN8A, SGCE, SLC16A2, SLC2A1, SLC30A10, SLC6A3, SPR, SUCLA2, TAF1, TH, THAP1, TOR1A, TUBB4A |
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Discinesia, Paroxística / Distonia |
Painel por Sequenciamento de Próxima Geração |
ADCY5, DLAT, KCNMA1, PDHA1, PDHX, PNKD |
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Angelman, Síndrome, Diagnósticos Diferenciais |
Painel por Sequenciamento de Próxima Geração |
ARID1B, ARX, ATRX, CDKL5, CNTNAP2, DDX3X, DYRK1A, EHMT1, FOXG1, HERC2, KDM5C, KIAA2022, MBD5, MECP2, MEF2C, NRXN1, PDHA1, SLC6A8, SLC9A6, SYNGAP1, TCF4, UBE3A, ZEB2 |
