Clinical Indication ID & Name
R169
Acute intermittent porphyria
Test Group
Gastrohepatology
Test code
R169.1
Test name
N/A
Target genes
HMBS
Test scope
n/a
Test method/ technology
Single gene sequencing >=10 amplicons
Optimal Family Structure
n/a
Eligibility Criteria
Clinical features of acute intermittent porphyria (AIP), AND ALA, PBG, or total porphyrin testing suggests diagnosis of AIP
Commissioning group
HSS/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