Next Generation Sequencing | Deletion / Duplication | NGS & Del Dup Comprehensive |
---|---|---|
Price: $950
|
Price: $750
|
Price: $1600
|
CPT: 81406
|
CPT: 81404
|
CPT: 81406
81404
|
Ganglioside GM3 synthase deficiency is a rare autosomal recessive infantile-onset symptomatic epilepsy syndrome associated with developmental stagnation and cortical blindness. The ST3GAL5 gene product functions as a GM3 synthase. Affected children completely lack GM3 and its downstream biosynthetic derivatives but have increased levels of the immediate precursor to GM3, lactosylceramide.
Type E
4 weeks or less