MSX1 Sequencing

Patients with Witkop syndrome have varying degrees of missing teeth and poorly formed fingernails and toenails. It is inherited in an autosomal dominant manner. Orofacial Cleft 5 is nonsyndromic and presents with varying degrees of cleft lip with and without cleft palate. Tooth Agenesis is characterized by oligodontia. 75% of patients with mutations in MSX1 have absence of the maxillary first premolars. These conditions are inherited in an autosomal dominant manner. This laboratory performs Sanger sequencing of the MSX1 gene.

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Test Code
S0900

Turn Around Time
3-5 weeks

Billing

CPT Code
81479×1

Ordering Guidance

If there are questions regarding this test, please contact Client Services at 617-553-5880 or clientservices@claritasgenomics.com

Details

Genes Covered
MSX1

Methods
Sanger