Dermato-NGS

Doenças dermatológicas: sequenciamento - 151 genes

Painel ampliado para a investigação de genes previamente previamente associados a doenças neurocutâneas, albinismo oculocutâneo, displasia ectodérmica, ictioses, queratoses, hipertricose não síndrômica, epidermólise bolhosa, entre outros.

AAGAB, ABCA12, ABHD5, ALAS2, ALDH3A2, ALOX12B, ALOXE3, ANAPC1, AP1S1, AP3B1, AP3D1, APCDD1, AQP5, ATP2C1, BLOC1S3, BLOC1S6, C10orf11, CARD11, CARD14, CAST, CD151, CDH3, CDSN, CERS3, CLDN1, COL17A1, COL7A1, CSTA, CTSC, CYP4F22, DOCK8, DSC2, DSG1, DSG4, DSP, DST, DTNBP1, EBP, EDA, EDAR, EDARADD, ELOVL1, ELOVL4, ENPP1, EXPH5, FECH, FERMT1, FLG, FLG2, FRMD7, GJA1, GJB2, GJB3, GJB4, GJB6, GPR143, HOXC13, HPS1, HPS3, HPS4, HPS5, HPS6, HR, IKBKG, IL36RN, ITGA3, ITGA6, ITGB4, JUP, KANK2, KDSR, KLHL24, KRT1, KRT10, KRT14, KRT16, KRT17, KRT2, KRT25, KRT5, KRT6A, KRT6B, KRT6C, KRT74, KRT85, KRT9, LAMA3, LAMB3, LAMC2, LIPH, LIPN, LOR, LPAR6, LRMDA, LTBP3, LYST, MBTPS2, MLPH, MSX1, MVK, MYO5A, NCSTN, NECTIN1 (PVRL1), NECTIN4 (PVRL4), NFKB2, NFKBIA, NIPAL4, OCA2, PAX9, PEX7, PGM3, PHYH, PKP1, PLEC, PNPLA1, POMP, PORCN, PSEN1, PSENEN, RAB27A, RHBDF2, RMRP, RSPO1, RSPO4, SDR9C7, SERPINB7, SERPINB8, SLC24A5, SLC27A4, SLC38A8, SLC45A2, SLURP1, SNAP29, SPINK5, ST14, STAT3, STS, SULT2B1, SUMF1, TAT, TGM1, TGM5, TP63, TRPV3, TSPEAR, TYR, TYRP1, UVSSA, VPS33B, WNT10A, ZMPSTE24

40503801

40 a 60 dias úteis

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