Next Generation Sequencing | Deletion / Duplication | NGS & Del Dup Comprehensive |
---|---|---|
Price: $1500
|
Price: $750
|
Price: $2150
|
CPT: 81408
|
CPT: 81407
|
CPT: 81408
81407
|
Cohen syndrome is an autosomal recessive disorder associated with the VPS13B gene. It is characterized by nonprogressive mild to severe psychomotor retardation, motor clumsiness, microcephaly, characteristic facial features, childhood hypotonia and joint laxity, progressive retinochoroidal dystrophy, myopia, intermittent isolated neutropenia, and a cheerful disposition.
Type E
4 weeks or less