Clinical Indication ID & Name
NIPD for spinal muscular atrophy - mutation testing
Test Group
NIPD
Specialties
Test code
R311.1
Test name
N/A
Target genes
SMN1
Test scope
n/a
Test method/ technology
NIPD
Optimal Family Structure
n/a
Eligibility Criteria
1. Pregnancy at risk of spinal muscular atrophy due to known SMN1 mutation(s) for which NIPD by
mutation testing is required following discussion with testing laboratory, AND
2. Both parents confirmed to be carriers
Commissioning group
Specialised
Overlapping idications
n/a
Address for samples/request forms
Genetics Laboratory
5th Floor Tower Wing
Guy’s Hospital
London
SE1 9RT
Contact with queries
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/
Request form download
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