Request / Find a Test Tool

The National Genomic Test Directories specify which genomic tests are commissioned by the NHS in England, to be delivered by Genomic Laboratory Hubs.

This tool allows clinical teams to search all of the genomic tests available to patients through the National Testing Directory. From here you can find out more details about each test and information about how to order them. These tests can only be ordered by clinical teams, if you are a patient looking to request a test please speak to your clinical team directly.

Childhood onset hereditary spastic paraplegia

Clinical Indication ID & Name

R61

Childhood onset hereditary spastic paraplegia

Test Group

Neurology

Specialties

Clinical Genetics Metabolic Medicine Neurology

Test code

R61.3

Test name

N/A

Target genes

Hereditary spastic paraplegia - Childhood onset (568) STR

Test scope

n/a

Test method/ technology

STR testing

Optimal Family Structure

n/a

Eligibility Criteria

Unexplained spastic paraplegia of likely monogenic aetiology with onset in childhood

Test code

R61.4

Test name

N/A

Target genes

Hereditary spastic paraplegia - Childhood onset (568)

Test scope

n/a

Test method/ technology

WGS

Optimal Family Structure

n/a

Eligibility Criteria

Unexplained spastic paraplegia of likely monogenic aetiology with onset in childhood

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

gos-tr.norththamesgenomics@nhs.net

Supporting documents

Rare Disese WGS Clinician pack

Education resources

n/a

Service updates

n/a

Request form download

RD WGS request form

Consent record

See consent guidance in test request form

Sample requirements

See sample guidance in test request form