Clinical Indication ID & Name
R19
Autoimmune lymphoproliferative syndrome with defective apoptosis
Test Group
Immunology
Specialties
Test code
R19.1
Test name
N/A
Target genes
FAS
Test scope
n/a
Test method/ technology
Single gene sequencing >=10 amplicons
Optimal Family Structure
n/a
Eligibility Criteria
Lymphoproliferative syndrome or other lymphoproliferative disorders consistent with FAS-related disease with:
• abnormal Fas-mediated apoptosis, OR
• elevated alpha beta double negative T cells, OR
• elevated sFAS, OR
• elevated Vitamin B12
Commissioning group
Specialised
Overlapping idications
• R15 Primary immunodeficiency panel test should be used where clinical and laboratory features are not typical and a broader range of genes are potentially causative
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