Exames Genéticos > Encefalo-NGS Voltar
 
 
Código
Encefalo-NGS
Doença(s)
Doenças cerebrovasculares: sequenciamento - 416 genes
Gene / Região
AARS, ABAT, ACOX1, ACTA2, ACVRL1, ADAR, ADCY5, ADSL, AIMP1, AKT1, AKT3, ALDH5A1, ALDH7A1, ALG1, ALG11, ALG13, ALG3, ALG6, ALG8, ALG9, ALPL, AMPD2, AMT, AP3B2, ARFGEF2, ARG1, ARHGEF9, ARID1B, ARV1, ARX, ASPA, ATL1, ATL3, ATN1, ATP1A1, ATP1A2, ATP1A3, ATP2A1, ATP6V0A2, ATP7A, ATP7B, ATR, ATRX, B3GLCT (B3GALTL), BCKDHA, BCKDHB, BCS1L, BOLA3, BRAF, BRAT1, BSCL2, BTD, C12orf57, CACNA1A, CACNA1D, CACNA1E, CACNA1G, CACNA1S, CACNB4, CASK, CC2D2A, CCM2, CDKL5, CEP152, CHD2, CHRNA2, CHRNA4, CHRNB2, CIC, CLCN1, CLCN4, CLN3, CLN8, CNKSR2, CNNM2, CNTNAP2, COG7, COL18A1, COL3A1, COL4A1, COL4A2, COQ2, COQ4, COQ8A (ADCK3), COQ8B (ADCK4), COQ9, CPA6, CREBBP, CSTB, CTSD, D2HGDH, DCX, DDX3X, DEAF1, DENND5A, DEPDC5, DHCR7, DHDDS, DIAPH1, DNM1, DNM1L, DOCK7, DPAGT1, DPM1, DPYD, DYNC1H1, DYRK1A, EARS2, EEF1A2, EFTUD2, EHMT1, EIF2B2, EIF2B4, EIF2B5, EIF2S3, ELN, EML1, EMX2, ENG, EPG5, EPM2A, ETHE1, EXOSC3, FAR1, FARS2, FBXL4, FBXO11, FGFR3, FH, FKTN, FLNA, FLVCR2, FOLR1, FOXG1, FRRS1L, FUCA1, FUT8, GABBR2, GABRA1, GABRB3, GABRG2, GALC, GAMT, GBA, GCH1, GFAP, GFM1, GLA, GLB1, GLDC, GLRA1, GLRB, GLUD1, GLUL, GLYCTK, GM2A, GNAO1, GNAQ, GNB5, GOSR2, GPHN, GRIN1, GRIN2A, GRIN2B, GSS, GUCY1A3, HACE1, HAX1, HBB, HCFC1, HCN1, HCN2, HEPACAM, HEXA, HLCS, HMGCL, HNRNPU, HRAS, HSD17B4, HTRA2, IDH2, IER3IP1, IFIH1, IKBKG, IQSEC2, ITPA, JAG1, KARS, KCNA1, KCNA2, KCNB1, KCNC1, KCNJ10, KCNJ11, KCNJ2, KCNQ2, KCNQ3, KCNQ5, KCNT1, KCTD3, KCTD7, KIF1A, KIF2A, KIF5C, KRAS, KRIT1, LARGE1 (LARGE), LGI1, LIAS, LYST, MACF1, MAF, MAGI2, MAP2K1, MAP2K2, MBD5, MBOAT7, MDH2, MECP2, MED12, MEF2C, MFF, MFSD8, MLC1, MMACHC, MMADHC, MOCS1, MOCS2, MOGS, MPDU1, MTHFR, MTOR, MTR, NAGA, NARS2, NDE1, NDUFA1, NDUFA10, NDUFAF2, NDUFAF5, NDUFS4, NDUFS8, NDUFV1, NF1, NGF, NGLY1, NHLRC1, NOTCH3, NRXN1, NSD1, NSDHL, NTRK1, NTRK2, OCLN, OPHN1, PACS1, PAFAH1B1, PAH, PCCA, PCCB, PCDH19, PCNT, PDCD10, PDHA1, PDHX, PET100, PEX1, PEX10, PEX12, PEX13, PEX19, PEX2, PEX3, PEX6, PEX7, PHACTR1, PHGDH, PIGA, PIGN, PIGO, PIGT, PIGW, PIK3CA, PIK3R2, PKD1, PKD2, PLCB1, PMM2, PNKD, PNKP, PNPO, POLG, POMGNT1, POMGNT2 (GTDC2), POMT1, PPP3CA, PPT1, PRICKLE1, PRMT7, PRNP, PRODH, PRRT2, PSAP, PTEN, PTPN23, PTS, PURA, PYGM, QARS, QDPR, RAB18, RAB7A, RANBP2, RARS2, RASA1, RELN, RFT1, RMND1, RNASEH2A, RNASEH2B, RNASEH2C, RNASET2, ROGDI, RORA, RTTN, RYR1, SAMHD1, SCARB2, SCN10A, SCN11A, SCN1A, SCN1B, SCN2A, SCN3A, SCN4A, SCN8A, SCN9A, SCO1, SCO2, SEPSECS, SEPT9, SETBP1, SETD5, SLC12A5, SLC13A5, SLC16A2, SLC1A2, SLC1A3, SLC25A1, SLC25A12, SLC25A22, SLC2A1, SLC2A10, SLC35A2, SLC6A1, SLC6A19, SLC6A5, SLC6A8, SLC9A6, SMAD3, SMAD4, SMARCA2, SMS, SPR, SPTAN1, SPTLC1, SPTLC2, ST3GAL5, STAG1, STAMBP, STRADA, STX1B, STXBP1, SUCLA2, SUOX, SURF1, SYN1, SYNGAP1, SYNJ1, SZT2, TBC1D24, TBCK, TBL1XR1, TCF4, TGFB2, TGFBR1, TGFBR2, TMEM70, TPP1, TRAK1, TREX1, TRPA1, TRPM6, TSC1, TSC2, TSEN2, TSEN54, TTR, TUBA1A, TUBB2A, TUBB2B, TUBB3, TUBB4A, TUBG1, TWNK (C10orf2), UBE2A, UBE3A, UNC80, WDR45, WDR45B, WDR62, WDR73, WNK1, WWOX, ZBTB18 e ZEB2
TUSS
40503801
Prazo de entrega
60 a 90 dias
Preço
R$ 2.790,00

Como solicitar o exame?


  • Entre em contato conosco por e-mail.
  • O médico e o paciente devem preencher os seguintes formulários:
    • Instrução para coleta - individual - 2017 - Fazer download
    • Formulário para Diagnóstico Molecular - Fazer download
    • Termo de consentimento geral - Fazer download
  • Envie as amostras pelos Correios ou entre em contato para realizar a coleta em nosso laboratório.

Informações sobre o exame:


O painel compreende 416 genes previamente associados a encefalopatias epiléticas, epilesia focal familial, epilepsia generalizada, síndromes de dor, canalopatias cerebrais, síndrome de Rett, síndrome de Dravet, CADASIL, CARASIL, entre outras.

Entre em contato para solicitar o exame:


  • E-mail: especialista_cegh@ib.usp.br
    (em horário comercial)