NGS Craniosynostosis Panel


Disorder Craniosynostosis
Gene Names FGFR1
Clinical info

Craniosynostosis involves premature or disordered suture closure resulting in skull asymmetry. This condition occurs in approximately 1 in 2500 births, and most are inherited from an affected parent or occur as a de novo autosomal dominant mutation. However, a few of these conditions result from autosomal recessive inheritance including Antley-Bixler, Carpenter, and Baller-Gerold syndromes. Craniosynostosis syndromes exhibit genetic heterogeneity as well as phenotypic variability with features that may include facial dysmorphism, palatal abnormalities, short stature, proptosis, and developmental delays. Craniosynostosis may also occur as an isolated finding. The 8 genes included on this panel account for multiple distinct clinical phenotypes. Click on the link below to see a list of associated conditions for these genes.

List of Genes & Associated Clinical Phenotypes

Indications Molecular testing is useful to confirm the diagnosis and to identify the disease causing mutations within a family to allow for carrier testing and prenatal diagnosis.
Detection The current design of the craniosynsotosis panel covers the coding region for all 8 genes and the flanking intronic sequences. This method allows for analysis of greater than 98% of the targeted sequence for the detection of nucleotide substitutions and small deletions and duplications. Large deletions and duplications will not be detected by this panel. Mutations and variants identified on the panel are confirmed with Sanger sequencing. All novel and apparently pathogenic changes are reported when found within the coding region as well as within 10 basepairs of each intron/exon boundary for each gene. Promoter and 3' untranslated sequences are not included in the current analysis. It should be noted that the current protocol is not specifically designed to detect copy number alterations and single exon deletions may require additional follow-up to determine whether or not they represent technical artifacts.

We recommend further array-based testing to more accurately address the concerns of dosage alterations. The Cytogenetic Laboratory at GGC offers a high resolution testing whole genome SNP microarray. The GGC Diagnostic Laboratory Directors are available for further consultation regarding the limitations of the NGS and array testing procedures.
Associated Tests

The following genes in this panel can also be requested as individual sequencing tests:
FGFR2 (selected exons)
(selected exons)

Effective January 1, 2017, all NGS panels are performed on an exome backbone with the potential for reflex to whole exome sequencing at a reduced cost. Please contact the laboratory to discuss the requirements for exome sequencing.

Specimen Requirements 5 to 10 ml of peripheral blood collected in an EDTA (lavender top) Vacutainer tube is preferred. The minimal blood needed for reliable DNA isolation is 3 ml.

For prenatal specimens, we can accept chorionic villi, amniotic fluid, or cultured flasks from a CVS or amniocentesis. We are not performing any direct analysis at this time. For cultured flasks, please send 2x T25 flasks of confluent cells.
Transport The specimen should be kept at room temperature and delivered via overnight shipping. FedEx is preferred. If shipment is delayed by one or two days, the specimen should be refrigerated and shipped at room temperature. Do not freeze the specimen.  Samples collected on Friday can be safely designated for Monday delivery.
Turnaround time 8-10 weeks
Prenatal testing The panel can be performed on prenatal specimens when there are suggestive ultrasound findings of craniosynostosis. Please be aware that due to the current turnaround time for this test, it is unlikely results will be available in time for families to use this information for pregnancy management. These results will be most helpful for families interested in recurrence risk information.

If the pathogenic mutation(s) are identified in an affected individual using this panel, prenatal diagnosis is available for future pregnancies. Sanger sequencing will be used for prenatal diagnosis when there is a known familial mutation. Additional fees for cell culture and maternal cell contamination may apply. Maternal cell contamination studies are required for all prenatal molecular tests. Contact the laboratory prior to sending a prenatal specimen.

CPT Codes 81479
Cost $3000

Insurance billing is available for this test. The Insurance Billing Form is required along with copies of the authorization or letter of agreement from the insurance company.
Contact For further information contact one of our This email address is being protected from spambots. You need JavaScript enabled to view it. at 1-800-473-9411.

Molecular Diagnostic Lab

The Molecular Diagnostic Lab offers DNA analysis for many genetic disorders via gene sequencing, targeted mutation analysis, MLPA deletion/duplication testing, trinucleotide repeat analysis and next generation sequencing panels.

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