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Year Number of Results
2019 18
2020 22
2021 18
2022 30
2023 21
2024 8

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Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes.
Nosé V, Lazar AJ. Nosé V, et al. Head Neck Pathol. 2022 Mar;16(1):143-157. doi: 10.1007/s12105-022-01414-z. Epub 2022 Mar 21. Head Neck Pathol. 2022. PMID: 35312981 Free PMC article. Review.
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head and neck region, as Gorlin syndrome/nevoid basal cell carcinoma syndrome associated with odontogenic keratocysts; Brooke-Spiegler syndrome/fa …
This review highlights the important findings within these syndromes, especially on the update on syndromes with tumors involving the head a …
WWP1 Gain-of-Function Inactivation of PTEN in Cancer Predisposition.
Lee YR, Yehia L, Kishikawa T, Ni Y, Leach B, Zhang J, Panch N, Liu J, Wei W, Eng C, Pandolfi PP. Lee YR, et al. N Engl J Med. 2020 May 28;382(22):2103-2116. doi: 10.1056/NEJMoa1914919. N Engl J Med. 2020. PMID: 32459922 Free PMC article.
Such mutations have been associated with a hereditary predisposition to multiple types of cancer, including the Cowden syndrome. However, a majority of patients who have PHTS-related phenotypes have tested negative for PTEN mutations. ...
Such mutations have been associated with a hereditary predisposition to multiple types of cancer, including the Cowden syndrome …
Cowden Syndrome.
Balthazar P, Klontzas ME, Heng LXX, Kearns C. Balthazar P, et al. Radiographics. 2022 Mar-Apr;42(2):E44-E45. doi: 10.1148/rg.210230. Epub 2022 Feb 18. Radiographics. 2022. PMID: 35179988 No abstract available.
Dermal hyperneury.
Marušić Z, Korša L, Calonje E. Marušić Z, et al. Clin Dermatol. 2021 Mar-Apr;39(2):291-294. doi: 10.1016/j.clindermatol.2020.10.008. Epub 2020 Oct 16. Clin Dermatol. 2021. PMID: 34272024
The syndromes most commonly associated with DN include multiple endocrine neoplasia 2B and 2A, neurofibromatosis type II, and Cowden syndrome. Patients with syndrome-associated DN have an increased risk for various malignancies. ...
The syndromes most commonly associated with DN include multiple endocrine neoplasia 2B and 2A, neurofibromatosis type II, and Cowden …
Cowden syndrome.
Wadia R. Wadia R. Br Dent J. 2021 Mar;230(6):362. doi: 10.1038/s41415-021-2852-z. Br Dent J. 2021. PMID: 33772192 No abstract available.
Cowden Syndrome.
Dickerson T, Poche W, Meaux T. Dickerson T, et al. Skinmed. 2021 Feb 1;19(1):69-71. eCollection 2021. Skinmed. 2021. PMID: 33658120
Cowden Disease: A Review.
Magaña M, Landeta-Sa AP, López-Flores Y. Magaña M, et al. Am J Dermatopathol. 2022 Oct 1;44(10):705-717. doi: 10.1097/DAD.0000000000002234. Am J Dermatopathol. 2022. PMID: 36122333 Review.
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. Cowden syndrome is included in this syndrome . PTEN (phosphatase and tensin homolog) is a tumor suppressor gene located on chromosome 10q22-23; nearly 60%-90% …
PTEN hamartoma tumor syndrome (PTHS) includes diseases with germline pathogenic variants in the PTEN gene. Cowden syndrome is …
Hamartomatous polyps: Diagnosis, surveillance, and management.
Gorji L, Albrecht P. Gorji L, et al. World J Gastroenterol. 2023 Feb 28;29(8):1304-1314. doi: 10.3748/wjg.v29.i8.1304. World J Gastroenterol. 2023. PMID: 36925460 Free PMC article. Review.
These syndromes exhibit hamartomatous gastrointestinal polyps in conjunction to extra-intestinal manifestations, which require conscientious and diligent monitoring. Peutz-Jeghers syndrome, Cowden syndrome, and juvenile polyposis syndrome are the most common display …
These syndromes exhibit hamartomatous gastrointestinal polyps in conjunction to extra-intestinal manifestations, which require conscientious …
The Cowden Syndrome.
Molière S, Mathelin C. Molière S, et al. N Engl J Med. 2020 Apr 9;382(15):e29. doi: 10.1056/NEJMicm1910478. N Engl J Med. 2020. PMID: 32268030 No abstract available.
PTEN Hamartoma tumor syndrome in childhood: A review of the clinical literature.
Macken WL, Tischkowitz M, Lachlan KL. Macken WL, et al. Am J Med Genet C Semin Med Genet. 2019 Dec;181(4):591-610. doi: 10.1002/ajmg.c.31743. Epub 2019 Oct 14. Am J Med Genet C Semin Med Genet. 2019. PMID: 31609537 Review.
PHTS incorporates a number of historical clinical presentations including Bannayan-Riley-Ruvalcaba syndrome, Cowden syndrome, and a macrocephaly-autism/developmental delay syndrome. ...
PHTS incorporates a number of historical clinical presentations including Bannayan-Riley-Ruvalcaba syndrome, Cowden syndrome, …
97 results