Genetic Test Details
Hereditary Spastic Paraplegia: Comprehensive
Test Information
- Titre
-
Hereditary Spastic Paraplegia: Comprehensive
- Catégorie
- Neurogenetics
- Sub Category
-
Hereditary Spastic Paraplegia
- Gene/Platform/Region List
-
ABCD1, ADAR, ALDH18A1, ALS2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, ATL1, ATP13A2, B4GALNT1, BSCL2, C19orf12, CAPN1, CPT1C, CYP2U1, CYP7B1, DDHD1, DDHD2, ERLIN1, ERLIN2, FA2H, FAR1, FARS2, GBA2, HACE1, HPDL, HSPD1, IBA57, IFIH1, KIDINS220, KIF1A, KIF1C, KIF5A, L1CAM, MAG, MTRFR, NIPA1, NT5C2, PCYT2, PLP1, PNPLA6, POLG, POLR3A, POLR3B, REEP1, REEP2, RNF170, RTN2, SACS, SELENOI, SETX, SLC16A2, SPART, SPAST, SPG11, SPG21, SPG7, TECPR2, TFG, TUBB4A, UBAP1, UCHL1, VPS13D, WASHC5, ZFYVE26
- Test type
- Gene Panel
- Samples Accepted
- Blood , DNA
- Indications
- Diagnostics , Prenatal
- Test Methodology
- CNV , Sequencing
- Methodology Notes
-
Exome + targeted microarray
- Disease/Condition
-
Hereditary Spastic Paraplegia
Dernière Mise à Jour: 18 juin 2025