Clinical Indication ID & Name
R87
Cerebral malformation
Test Group
Neurology
Specialties
Test code
R87.2
Test name
N/A
Target genes
Genomewide
Test scope
n/a
Test method/ technology
Microarray
Optimal Family Structure
n/a
Eligibility Criteria
Cerebral malformation such as cortical malformation or porencephaly with features suggestive of a monogenic cause
Test code
R87.3
Test name
N/A
Target genes
Cerebral malformations (491)
Test scope
n/a
Test method/ technology
WGS
Optimal Family Structure
n/a
Eligibility Criteria
Cerebral malformation such as cortical malformation or porencephaly with features suggestive of a monogenic cause
Commissioning group
Specialised
Overlapping idications
• R110 Segmental overgrowth disorders – Deep sequencing test should be used where megalencephaly is present to allow detection of mosaic mutations
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