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Seminars in Colon and Rectal Surgery, ISSN 1043-1489, 09/2018, Volume 29, Issue 3, pp. 120 - 123
Hamartomatous polyps of the gastrointestinal tract are one of the major clinical features for several hereditary syndromes. Juvenile polyposis syndrome,... 
PTEN | Peutz–Jeghers | Hamartomatous polyp | Juvenile polyposis
Journal Article
American Journal of Gastroenterology, ISSN 0002-9270, 02/2015, Volume 110, Issue 2, pp. 223 - 262
Journal Article
Gut, ISSN 0017-5749, 07/2010, Volume 59, Issue 7, pp. 975 - 986
Journal Article
MEDICINE, ISSN 0025-7974, 07/2019, Volume 98, Issue 27, p. e16381
Rationale: Peutz-Jeghers syndrome (PJS) is currently defined as an inherited condition, also called a familial hamartomatous polyposis syndrome, characterized... 
follow-up | MEDICINE, GENERAL & INTERNAL | diagnosis | POLYPOSIS | Peutz-Jeghers syndrome | Humans | Endoscopy, Gastrointestinal | Male | Peutz-Jeghers Syndrome - diagnosis | Peutz-Jeghers Syndrome - genetics | Child | Peutz-Jeghers Syndrome - surgery | Medical research | Gastrointestinal system | Medicine, Experimental | Research | Diagnosis | Health aspects
Journal Article
Endoscopy, ISSN 0013-726X, 2015, Volume 47, Issue 4, pp. 352 - 376
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2017, Volume 217, Issue 5, pp. 512 - 521
The world of hereditary cancers has seen exponential growth in recent years. While hereditary breast and ovarian cancer and Lynch syndrome account for the... 
Obstetrics and Gynecology | BRCA | risk reduction | screening | ovarian cancer | high risk | endometrial cancer | hereditary cancer | cervical cancer | Lynch syndrome | BRCA2 MUTATION CARRIERS | LI-FRAUMENI SYNDROME | LYNCH-SYNDROME | COLORECTAL-CANCER SYNDROME | PEUTZ-JEGHERS-SYNDROME | RANDOMIZED-TRIAL | REDUCING SALPINGO-OOPHORECTOMY | FAMILIAL OVARIAN-CANCER | OBSTETRICS & GYNECOLOGY | GERMLINE MUTATIONS | Genetic Testing | DNA Polymerase III - genetics | Hereditary Breast and Ovarian Cancer Syndrome - diagnosis | Humans | Li-Fraumeni Syndrome - diagnosis | DNA Mismatch Repair - genetics | Tumor Suppressor Protein p53 - genetics | Genital Neoplasms, Female - diagnosis | Li-Fraumeni Syndrome - genetics | Epithelial Cell Adhesion Molecule - genetics | Genes, BRCA2 | Female | RNA Helicases - genetics | Lynch Syndrome II - genetics | Neoplastic Syndromes, Hereditary - genetics | Genes, BRCA1 | Genital Neoplasms, Female - genetics | Hereditary Breast and Ovarian Cancer Syndrome - genetics | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease | Hamartoma Syndrome, Multiple - genetics | Fanconi Anemia Complementation Group Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | Neoplastic Syndromes, Hereditary - diagnosis | MutS Homolog 2 Protein - genetics | DNA-Binding Proteins - genetics | Peutz-Jeghers Syndrome - genetics | Hamartoma Syndrome, Multiple - diagnosis | MutL Protein Homolog 1 - genetics | Peutz-Jeghers Syndrome - diagnosis | Lynch Syndrome II - diagnosis | Mismatch Repair Endonuclease PMS2 - genetics | Gene mutations | Endometrial cancer | Diagnosis | Cervical cancer | Genetic screening | Cancer | Ovarian cancer
Journal Article
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2015, Volume 213, Issue 2, pp. 161 - 165
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 01/2019, Volume 380, Issue 5, pp. 472 - 472
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 2017, Volume 23, Issue 13, pp. e107 - e114
Journal Article
Journal Article
The Oncologist, ISSN 1083-7159, 07/2012, Volume 17, Issue 7, pp. 886 - 887
This commentary highlights the potential for early diagnosis of certain cancers diagnoses for individuals with hereditary faciocutaneous disorders. 
ONCOLOGY | PEUTZ-JEGHERS-SYNDROME | TUBEROUS-SCLEROSIS | FEATURES | Costello Syndrome - genetics | Costello Syndrome - pathology | Costello Syndrome - diagnosis | Humans
Journal Article
Journal Article