PTEN Sequencing

Test Background

PTEN Hamartoma Tumor Syndrome (PHTS) includes Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba (BRR), Proteus syndrome (PS), and Proteus-like syndrome. CS is characterized by benign and malignant tumors of the breast, thyroid, and endometrium. Individuals with CS typically have macrocephaly and have an increased chance for developing breast, thyroid, and endometrial cancer. BRR is characterized by macrocephaly, intestinal hamartomatous polyposis, lipomas, and pigmented macules of the glans penis. PS includes hamartomatous overgrowth of multiple tissues as well as nevi of the connective tissue and epidermis. Proteus-like syndrome refers to individuals with features of PS, but who do not meet diagnostic criteria. PHTS is inherited in an autosomal dominant manner. Approximately 85% of individuals meeting diagnostic criteria for CS and 65% clinically diagnosed with BRR have a PTEN mutation. Data suggest that 50% of individuals with PS and 20% with Proteus-like syndrome have detectable mutations. Individuals with autism and macrocephaly have also been identified with PTEN mutations especially if there is a family history consistent with CS or BRR. This laboratory performs both Sanger sequencing and deletion/duplication by MLPA.

Gene(s)

PTEN

About Claritas

Claritas Genomics serves children affected with complex genetic disorders by providing timely and accurate results, resolving families’ long search for answers. By combining clinical expertise of the world’s best pediatric specialists with innovative platform solutions, Claritas is working to improve patient care and enable new discoveries. We are committed to the highest quality and accessibility of information and our interpretive services and unique approach to reporting set the standard for reliably and clearly communicating genetic information.

Now is the time to integrate genomics into clinical practice to inform, guide and improve medical treatment for kids around the world.