Construct · 1 fields · 1 citations

PTEN hamartoma tumor syndrome: a standalone construct

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PTEN hamartomatumor syndrome1 CONSTRUCTPTEN hamartoma tumorPILARSKI · ONCOLOGY

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Oncology

a group of disorders caused by germline PTEN mutation, defined by revised major and minor clinical criteria including breast, thyroid and endometrial cancers and mucocutaneous lesions.

In oncology, PTEN hamartoma tumor syndrome refers to a group of disorders caused by germline PTEN mutation, defined by revised major and minor clinical criteria including breast, thyroid and endometrial cancers and mucocutaneous lesions. This meaning comes from Pilarski (2013) in JNCI Journal of the National Cancer Institute.[1]

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Nearby constructs

group4 fields · 4 citationsjingle · one word, four constructsminor3 fields · 3 citationsjingle · one word, three carriersmutation4 fields · 4 citationsjingle · one word, four constructs

References

  1. Pilarski, R., Burt, R., Kohlman, W., Pho, L., Shannon, K. M., & Swisher, E. (2013). Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria. JNCI Journal of the National Cancer Institute, 105(21), 1607-1616. https://doi.org/10.1093/jnci/djt277

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