Variant Names: 
Sensenbrenner syndrome

Cranioectodermal dysplasia (CED) is an autosomal recessive ciliopathy characterized by sagittal craniosynostosis, skeletal, facial and ectodermal abnormalities.read more

Tests Available

By gene: WDR35
Next Generation Sequencing
$990
Test Code: 1083
Deletion / Duplication
$990
Test Code: 1084
NGS/Del Dup Comprehensive
$1,365
Test Code: 1509

Related Panels
Skeletal dysplasia ciliopathy NGS panel (19 genes)
NGS $1,620
Del Dup $990
Comp $1,995
Craniosynostosis NGS panel (25 genes)
NGS $1,800
Del Dup $1,300
Comp $2,950

Test Details

Technical Information
Genes: 
WDR35
Disease Groups: 
Craniosynostosis and Craniofacial Disorders
Skeletal Ciliopathies
MIM: 
613610
Billing
Price: 
$990
CPT Codes: 
81479 x 1
Ordering
SKU:
1083
Turnaround Time: 
Typically 3 to 4 weeks from receipt of a sample in the laboratory. All cases involving ongoing pregnancies will be expedited.
Non-Prenatal Specimens: 
  1. Whole blood: purple-top (EDTA) tube, minimum of 3 ml
  2. Genomic DNA: minimum of 10 µg (at a concentration of at least 50 ng/µl)
  3. Fibroblasts: 4 confluent T-25 flasks
  4. Saliva: only samples collected in Oragene DNA Self-Collection Kit or Oragene Saliva Collection Kit for Young Children are accepted
Prenatal Specimens: 
  1. Cultured cells: 4 confluent T-25 flasks derived from amnio or CVS samples
  2. Genomic DNA: minimum of 10 µg (at a concentration of at least 50 ng/µl)
Shipping: 
Ship all specimen types at room temperature by overnight courier. Do not freeze.

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