| Literature DB >> 28476234 |
Joanne Ngeow1, Kaitlin Sesock2, Charis Eng3.
Abstract
Patients with PTEN hamartoma tumor syndrome (PHTS) may present to a variety of different subspecialties with benign and malignant clinical features. They have increased lifetime risks of breast, endometrial, thyroid, renal, and colon cancers, as well as neurodevelopmental disorders such as autism spectrum disorder. Patients and affected family members can be offered gene-directed surveillance and management. Patients who are unaffected can be spared unnecessary investigations. With longitudinal follow-up, we are likely to identify other non-cancer manifestations associated with PHTS such as metabolic, immunologic, and neurologic features.Entities:
Keywords: Cowden syndrome; PTEN; PTEN hamartoma tumor syndrome
Mesh:
Substances:
Year: 2017 PMID: 28476234 DOI: 10.1016/j.ecl.2017.01.013
Source DB: PubMed Journal: Endocrinol Metab Clin North Am ISSN: 0889-8529 Impact factor: 4.741