Order or find a test

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

Clinical Indication ID & Name

R231

Neuronal ceroid lipofuscinosis

Test Group

Metabolic

Test code

R231.1

Test name

N/A

Target genes

CLN3

Test scope

n/a

Test method/ technology

MLPA or equivalent

Optimal Family Structure

n/a

Eligibility Criteria

Clinical and laboratory features characteristic of Neuronal ceroid lipofuscinosis including presence of vacuolate lymphocytes, presence of pathological inclusions on tissue biopsy or enzyme deficiency

Test code

R231.2

Test name

N/A

Target genes

Neuronal ceroid lipofuscinosis (526)

Test scope

n/a

Test method/ technology

Small panel

Optimal Family Structure

n/a

Eligibility Criteria

Clinical and laboratory features characteristic of Neuronal ceroid lipofuscinosis including presence of vacuolate lymphocytes, presence of pathological inclusions on tissue biopsy or enzyme deficiency

Commissioning group

Specialised

Overlapping idications

• R271 Neuronal ceroid lipofuscinosis type 2 test should be considered where clinical features are specific to CLN2 • It is anticipated that many specific metabolic diagnoses will be made through use of broad genomic testing via the R98 Likely inborn error of metabolism - targeted testing is not possible early in the investigative pathway and in cases with atypical features where a broader differential diagnosis is under consideration

Address for samples/request forms

Genetics Laboratory
5th Floor Tower Wing
Guy’s Hospital
London
SE1 9RT

Contact with queries

gst-tr.southeastglh@nhs.net

Supporting documents

n/a

Education resources

n/a

Turn around times

All our turnaround times are listed on our specific turn around page https://southeastgenomics.nhs.uk/professionals/service-turn-around-times/

Consent record

See consent guidance in test request form

Sample requirements

Samples may be rejected for the following reasons: 1.Samples and request form do not show at least three identical patient identifiers 2.The sample is in the incorrect collection media 3.The request form is not sufficiently completed 4.The sample is not of sufficient volume 5.The sample is too old