Clinical Implications for Germline PTEN Spectrum Disorders

Joanne Ngeow, Kaitlin Sesock, Charis Eng*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

44 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)503-517
Number of pages15
JournalEndocrinology and Metabolism Clinics of North America
Volume46
Issue number2
DOIs
Publication statusPublished - Jun 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2017 Elsevier Inc.

ASJC Scopus Subject Areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Keywords

  • Cowden syndrome
  • PTEN
  • PTEN hamartoma tumor syndrome

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