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Primary Ciliary Dyskinesia Panel

Primary Ciliary Dyskinesia Panel

Regular price €29.00 EUR
Regular price Sale price €29.00 EUR
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This product is only meant for customers who already purchased a Dante Genome Test

Primary ciliary dyskinesia (PCD) is a rare condition characterized by chronic respiratory tract infections, abnormal positioning of internal organs and infertility. The clinical picture is determined by abnormalities in cilia and flagella, which are located in the lining of the airways, the reproductive system and other organs and tissues. Primary ciliary dyskinesia is caused by mutations in several genes; mutations in the DNAI1 and DNAH5 genes account for approximately 30 per cent of all cases.
This test may be indicated for those with a family history of Primary Ciliary Dyskinesia. Patients with congestion, situs inversus and frequent sinus and ear infections may also benefit. Genetic testing can help in diagnosis and in providing information on risks for other family members.

The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
  • Available in less than 24 hours
  • Based on Whole Genome Sequencing
  • 50 genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Ciliary dyskinesia, primary, 1, with or without situs inversus
  • Ciliary dyskinesia, primary, 2
  • Ciliary dyskinesia, primary, 9, with or without situs inversus
  • Ciliary dyskinesia, primary, 36, X-linked
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This product is only meant for customers who already purchased a Dante Genome Test