Clinical Indication ID & Name
R55
Hereditary ataxia with onset in childhood
Test Group
Neurology
Specialties
Test code
R55.3
Test name
N/A
Target genes
Hereditary ataxia and cerebellar anomalies - childhood onset (488) STR
Test scope
n/a
Test method/ technology
STR testing
Optimal Family Structure
n/a
Eligibility Criteria
Unexplained hereditary ataxia with onset in childhood including where differential diagnosis encompasses STR loci
Test code
R55.4
Test name
N/A
Target genes
Hereditary ataxia and cerebellar anomalies - childhood onset (488)
Test scope
n/a
Test method/ technology
WGS
Optimal Family Structure
n/a
Eligibility Criteria
Unexplained hereditary ataxia with onset in childhood including where differential diagnosis encompasses STR loci
Commissioning group
Specialised
Overlapping idications
n/a
Address for samples/request forms
North Thames GLH, Rare & Inherited Disease Genomic Laboratory
Specimen Reception, Level 5 Barclay House, 37 Queen Square,
London WC1N 3BH
Contact with queries
Supporting documents
Rare Disese WGS Clinician pack
Education resources
n/a
Service updates
n/a
Request form download
Consent record
See consent guidance in test request form
Sample requirements
See sample guidance in test request form