PAINEL DE DISTROFIA MUSCULARES, MIOPATIAS E MIASTE

O Painel de Distrofias Musculares, Miopatias e Miastenia avalia 80 genes:

ACTA1, AGRN, ANO5, B4GAT1, BAG3, BIN1, CAPN3, CAV3, CFL2, CHAT, CHKB, CHRNA1, CHRNB1, CHRND,

CHRNE, CNTN1, COL6A1, COL6A2, COL6A3, COLQ, CRYAB, DAG1, DES, DMD, DNAJB6, DNM2, DOK7,

DPAGT1, DPM1, DPM3, DYSF, EMD, FHL1, FKRP, FKTN, FLNC, GAA, GFPT1, GNE, HNRNPA1,

HNRNPA2B1, IGHMBP2, ISPD, ITGA7, KBTBD13, LAMA2, LARGE1, LDB3, LMNA, MAGEL2, MATR3,

MTM1, MUSK, MYH7, MYL2, MYOT, NEB, PLEC, PNPLA2, POMGNT1, POMT1, POMT2, PYGM,

RAPSN, RYR1, SELENON, SGCA, SGCB, SGCD, SGCG, SQSTM1, TCAP, TGFB1, TIA1, TNNT1,

TPM2, TPM3, TRIM32, TTN, VCP.

 

CONDIÇÕES

- Sangue total (EDTA).

 

VOLUME RECOMENDÁVEL

- 5,0 mL.

 

TEMPO DE JEJUM

- Jejum não obrigatório.

 

INTERFERENTES

- Uso de anticoagulante incorreto.