Next Generation Sequencing | Deletion / Duplication | NGS & Del Dup Comprehensive |
---|---|---|
Price: $950
|
Price: $750
|
Price: $1600
|
CPT: 81406
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CPT: 81405
|
CPT: 81406
81405
|
Neurodegeneration with brain iron accumulation type 1 (NBIA1), also known as Hallervorden-Spatz syndrome, is a rare, autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain. Clinical features include extrapyramidal dysfunction, onset in childhood and a relentlessly progressive course. NBIA1 is caused by mutations in the PANK2 gene, which encodes pantothenate kinase, the key regulatory enzyme in coenzyme-A biosynthesis.
Type E
4 weeks or less