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Leigh Syndrome Report

£49.00
Leigh Syndrome Report

Leigh Syndrome Report

£49.00
description

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

The Leigh Syndrome Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Leigh Syndrome, instead of a limited set of genes, like old genetic target panels.

Leigh Syndrome is a severe neurological disorder that usually becomes apparent in the first year of life. This condition is characterized by progressive loss of mental and movement abilities (psychomotor regression) and typically results in death within two to three years, usually due to respiratory failure.

Along with environmental factors, Genetics plays a key role in the regulation of Leigh Syndrome.

 

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

 

List of genes:

BCS1L
COX10
COX15
DLAT
DLD
LRPPRC
MT-ATP6
MT-CO3
MT-ND1
MT-ND2
MT-ND3
MT-ND4
MT-ND5
MT-ND6
MT-TI
MT-TK
MT-TL1
MT-TL2
MT-TV
MT TW
PC
PDHA1
PDHB
PDHX
SCN4A
SDHA
SURF1
TACO1
NDUFS3
NDUFS4
NDUFA10
NDUFA2
NDUFS8
NDUFA12
NDUFS7
NDUFV1
SERAC1
SLC19A3