Clinical Indication ID & Name
R201
Atypical haemolytic uraemic syndrome (139)
Test Group
Renal
Specialties
Test code
R201.1
Test name
N/A
Target genes
Atypical haemolytic uraemic syndrome (139)
Test scope
n/a
Test method/ technology
Small panel
Optimal Family Structure
n/a
Eligibility Criteria
Acute renal failure AND thrombocytopenia AND microangiopathic haemolytic anaemia (Coombs test negative), in a patient being considered for complement inhibitory therapies
Test code
R201.3
Test name
N/A
Target genes
CFH; CFHR1; CFHR3; CD46; CFI
Test scope
n/a
Test method/ technology
MLPA or equivalent
Optimal Family Structure
n/a
Eligibility Criteria
Acute renal failure AND thrombocytopenia AND microangiopathic haemolytic anaemia (Coombs test negative), in a patient being considered for complement inhibitory therapies
Commissioning group
Highly 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