Hereditary Spastic Paraplegia: Deletion & Duplication Analysis
Background
See related pages for information sheet on Hereditary Spastic Parapalegia
Clinical Significance
See related pages for information sheet on Hereditary Spastic Parapalegia
Test Name
Hereditary Spastic Paraplegia: Deletion & Duplication Analysis
Alternate Name/ Synonym
Hereditary Spastic Paraplegia
Test Code
HSP-Dosage
Division
Molecular Genetics
Method
Deletion & Duplication analysis by exon targeted microarray
Turn Around Time
4 weeks
Specimen Type
Blood; please contact the Genome Diagnostics Laboratory if you want to send gDNA. If sending a prenatal sample, please contact the laboratory prior to sending sample to discuss sample requirements.
For details about specimen requirements, please refer to: Specimen Types & Requirements (PDF).
Minimum Specimen Requirements
5-10 mL EDTA or ACD
0.5 mL EDTA (neonate); minimum 10 ug of DNA in 100 uL low TE (pH8.0)
Special Requirements
For more information, please see information sheet under specific condition.