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Journal of the American Academy of Dermatology, ISSN 0190-9622, 2013, Volume 68, Issue 2, pp. 189.e1 - 189.e21
Cutaneous findings are not uncommonly a concomitant finding in patients afflicted with gastrointestinal (GI) diseases. The dermatologic manifestations may... 
Cowden syndrome | hereditary and nonhereditary gastrointestinal malignancies | Muir-Torre syndrome | gastrointestinal disorders | hamartomatous polyposis syndrome | Cronkhite-Canada syndrome | Bannayan-Riley-Ruvalcaba syndrome | cutaneous manifestations | Peutz-Jeghers syndrome | Lynch syndrome | paraneoplastic syndrome | PEUTZ-JEGHERS-SYNDROME | RILEY-RUVALCABA-SYNDROME | HEREDITARY COLORECTAL-CANCER | DERMATOLOGY | PERIANAL PAGETS-DISEASE | LESER-TRELAT SIGN | MUIR-TORRE-SYNDROME | NECROLYTIC MIGRATORY ERYTHEMA | FAMILIAL ADENOMATOUS POLYPOSIS | PARANEOPLASTICA BAZEX-SYNDROME | MALIGNANT ACANTHOSIS NIGRICANS | Paraneoplastic Syndromes - genetics | Dermatomyositis - genetics | Carcinoma, Basal Cell - genetics | Colorectal Neoplasms - genetics | Humans | Hypotrichosis - genetics | Gastrointestinal Neoplasms - complications | Acanthosis Nigricans - genetics | Gastrointestinal Neoplasms - pathology | Skin Diseases, Genetic - etiology | Adenomatous Polyposis Coli - genetics | Histiocytoma, Benign Fibrous - genetics | PTEN Phosphohydrolase - genetics | Hamartoma Syndrome, Multiple - genetics | Necrolytic Migratory Erythema - diagnosis | Necrolytic Migratory Erythema - genetics | Intestinal Polyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Malignant Carcinoid Syndrome - genetics | Gastrointestinal Diseases - complications | Peutz-Jeghers Syndrome - genetics | Gastrointestinal Diseases - genetics | Paraneoplastic Syndromes - complications | Hamartoma Syndrome, Multiple - diagnosis | Skin Neoplasms - genetics | Skin Neoplasms - secondary | Colorectal Neoplasms, Hereditary Nonpolyposis - etiology | Mutation
Journal Article
Gene, ISSN 0378-1119, 05/2016, Volume 582, Issue 1, pp. 23 - 32
Numerous familial tumor syndromes are associated with distinctive oral mucosal findings, which may make possible an early diagnosis as an efficacious marker... 
Cowden syndrome | Odontogenic keratocystic tumors | Gardner syndrome | Peutz–Jeghers syndrome | Gorlin syndrome | Multiple endocrine neoplasia | Lynch/Muir–Torre syndrome | Ameloblastoma | Familial Adenomatous Polyposis (FAP) | Fordyce granules | Lynch/Muir-Torre syndrome | Peutz-Jeghers syndrome | LYNCH-SYNDROME | NONPOLYPOSIS COLORECTAL-CANCER | PEUTZ-JEGHERS-SYNDROME | COWDEN-DISEASE | Peutz-jeghers syndrome | GARDNERS-SYNDROME | MUIR-TORRE-SYNDROME | BASAL-CELL CARCINOMA | GENETICS & HEREDITY | MUCOCUTANEOUS PIGMENTATION | FAMILIAL ADENOMATOUS POLYPOSIS | Peutz-Jeghers Syndrome - pathology | Humans | Peutz-Jeghers Syndrome - therapy | Muir-Torre Syndrome - therapy | Muir-Torre Syndrome - pathology | Multiple Endocrine Neoplasia - genetics | Germ-Line Mutation - genetics | Molecular Targeted Therapy | Adenomatous Polyposis Coli - pathology | Adenomatous Polyposis Coli - complications | Adenomatous Polyposis Coli - therapy | Adenomatous Polyposis Coli - genetics | Mouth Mucosa - pathology | Gardner Syndrome - pathology | Genes, Tumor Suppressor | Gardner Syndrome - therapy | Gardner Syndrome - complications | Peutz-Jeghers Syndrome - complications | Peutz-Jeghers Syndrome - genetics | Multiple Endocrine Neoplasia - complications | Mouth Mucosa - metabolism | Muir-Torre Syndrome - genetics | Phenotype | Muir-Torre Syndrome - complications | Gardner Syndrome - genetics | Multiple Endocrine Neoplasia - therapy | Heterozygote | Multiple Endocrine Neoplasia - pathology | Genetic aspects | Gene mutations | Cancer
Journal Article
American Journal of Gastroenterology, ISSN 0002-9270, 02/2015, Volume 110, Issue 2, pp. 223 - 262
Journal Article
Archives of Pathology and Laboratory Medicine, ISSN 0003-9985, 12/2014, Volume 138, Issue 12, pp. 1685 - 1689
Journal Article
CANADIAN MEDICAL ASSOCIATION JOURNAL, ISSN 0820-3946, 03/2016, Volume 188, Issue 5, pp. E95 - E95
Muir-Torre syndrome is an autosomal dominant cancer syndrome expressed clinically as cutaneous tumours (sebaceous neoplasms or multiple keratoacanthomas) and... 
MEDICINE, GENERAL & INTERNAL | Sebaceous Gland Neoplasms - pathology | Humans | Middle Aged | Adenoma - pathology | Muir-Torre Syndrome - pathology | Female | Facial Neoplasms - pathology | Muir-Torre syndrome | Diagnosis | Research | Genetic testing | Biopsy | Genes | Cancer | Practice
Journal Article
Journal Article
Journal Article
PATHOLOGE, ISSN 0172-8113, 11/2019, Volume 40, Issue 6, pp. 584 - 591
Background. Hereditary nonpolyposis colorectal cancer (Lynch/HNPCC syndrome) is based on a germline mutation inducing increased occurrence of colorectal cancer... 
DIAGNOSIS | HNPCC | Hereditary nonpolyposis colorectal cancer | Lynch Syndrome | GENETICS | Germ-linemutation | PATHOLOGY | MEDICINE | Muir-Torre Syndrome | ADENOMAS | Repair protein | FAMILY
Journal Article