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Periodic Paralysis Report

$49.00

Periodic Paralysis Report

$49.00
description

 This product is only meant for customers who already 
purchased a Sequencing Test

Periodic Paralysis is a rare genetic disorder. It causes sudden attacks of short-term muscle weakness, stiffness, or paralysis.

The Periodic Paralysis Report is based on Whole Genome Sequencing Test. As such, it analyses all Common and Rare Variants associated with Periodic Paralysis. Hypokalemic Periodic Paralysis (HypoPP) is one of the periodic paralysis conditions; autosomal dominant genetic disorders caused by mutations in the sodium, potassium, and calcium channel genes in the skeletal muscle. In general, HypoPP is characterised by reversible attacks of muscle weakness coupled with decreased blood potassium concentrations.

Along with environmental factors, Genetics plays a key role in the regulation of Periodic Paralysis.

 

  • 100 genes analyzed
  • 100% genomic regions covered
  • Intragenic and intergenic regions analyzed
  • All variants reported


List of genes:

ACADVL
ADAMTS2
AGRN
ALG14
AMPD1
APOPT1
ATP1A2
B3GALT6
B4GALT7
C12ORF62
C1R
C1S
CACNA1A
CAV3
CHAT
CHRNA1
CHRNB1
CHRND
CHRNE
CHST14
CLCN1
CMTX1
CNBP
COA3
COA5
COA6
COL12A1
COL13A1
COL1A1
COL1A2
COL3A1
COL5A1
COL5A2
COLQ
COX10
COX14
COX15
COX20
COX6B1
CPT2
CYP11B1
CYP11B2
DOK7
DPAGT1
DSE
ENO3
FARS2
FASTKD2
FKBP14
FMR1
GAA
GFPT1
KCNE3
MTTS1
Kcnj18
KCNJ5
LDHA
LRP4
LRPPRC
MT-ATP6
MT-ATP8
MTCO1
MTCO2
MTCO3
MTTL1
MUSK
NOD2
PET100
PFKM
PGAM2
PGM1
PLEC
PLOD1
PMP22
POLG
PPPT2
PRDM5
PREPL
PYGM
RAPSN
RYR1
SCN1A
SCN4A
SCO1
SCO2
SLC12A3
SLC16A1
SLC39A13
SNAP25
SPR
SYT2
TACO1
TNFRSF1A
TNXB
ZNF469
KCNQ3
KCNQ5
CACNA1S
KCNJ2
ORAI1