Request / Find a Test Tool

The National Genomic Test Directories specify which genomic tests are commissioned by the NHS in England, to be delivered by Genomic Laboratory Hubs.

This tool allows clinical teams to search all of the genomic tests available to patients through the National Testing Directory. From here you can find out more details about each test and information about how to order them. These tests can only be ordered by clinical teams, if you are a patient looking to request a test please speak to your clinical team directly.

NIPD for FGFR3-related skeletal dysplasias – mutation testing

Clinical Indication ID & Name

R309

NIPD for FGFR3-related skeletal dysplasias - mutation testing

Test Group

NIPD

Test code

R309.1

Test name

N/A

Target genes

FGFR3

Test scope

n/a

Test method/ technology

NIPD

Optimal Family Structure

n/a

Eligibility Criteria

Pregnancy in which NIPD for FGFR3-related skeletal dysplasia is required
1. Abnormal ultrasound findings compatible with sonographic diagnosis of achondroplasia or other rare FGFR3-related skeletal dysplasia including Muenke syndrome, hypochondroplasia or hypochondroplasia with acanthosis nigricans:
a. Femoral length within the normal range at the routine 18-20-week scan, AND
b. Femur length and all long bones below the 3rd percentile after 25 weeks gestation, AND
c. Head circumference on or above 95th percentile or above the normal range for gestation at
diagnosis and/or frontal bossing present, AND
d. Fetal and maternal dopplers should be normal
e. Other features may include polyhydramnios or short fingers
OR
2. Abnormal ultrasound findings compatible with sonographic diagnosis of thanatophoric dysplasia or severe achondroplasia with developmental delay:
a. All long bones below the 3rd percentile from early pregnancy, AND
b. Small chest with short ribs, AND
c. At least one of: bowed femora, frontal bossing, cloverleaf skull, short fingers
OR
3. At risk pregnancy due to paternal FGFR3-related skeletal disorder OR a previous pregnancy with confirmed FGFR3-related skeletal disorder

Commissioning group

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

gos-tr.norththamesgenomics@nhs.net

Supporting documents

Rare Disese WGS Clinician pack

Education resources

n/a

Service updates

n/a

Consent record

See consent guidance in test request form

Sample requirements

See sample guidance in test request form