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04/2009
Aim: Report of a series of 12 cases of juvenile polyposis coli. Methods: The study period was from 1995 to 2005. All the patients were treated by total... 
juvenile polyposis syndrome | Ileal pouch | prophylactic surgery
Web Resource
Archives of Medical Science, ISSN 1734-1922, 2014, Volume 10, Issue 3, pp. 570 - 577
Juvenile polyposis syndrome (JPS) is an autosomal dominant predisposition to the occurrence of hamartomatous polyps in the gastrointestinal tract. Diagnosis of... 
Juvenile polyposis syndrome | Juvenile polyposis | SMAD4 gene | BMPR1A gene | SMAD4 | juvenile polyposis syndrome | PEUTZ-JEGHERS-SYNDROME | juvenile polyposis | PTEN | DELETION | COWDEN-SYNDROME | MEDICINE, GENERAL & INTERNAL | GENE | COLORECTAL-CANCER | COLI | GERMLINE MUTATIONS | BMPR1A | State of the Art Paper
Journal Article
Journal of Pediatric Gastroenterology and Nutrition, ISSN 0277-2116, 03/2019, Volume 68, Issue 3, pp. 453 - 462
Journal Article
International Journal of Surgery Case Reports, ISSN 2210-2612, 2019, Volume 59, pp. 73 - 75
Juvenile polyposis syndrome it is an uncommon autosomal dominant inherited condition. Hamartomatous polyps can affect the entire gastrointestinal tract but... 
Total gastrectomy | Endoscopic polypectomy | Juvenile polyposis
Journal Article
Journal Article
Human Pathology, ISSN 0046-8177, 2015, Volume 49, pp. 39 - 48
Journal Article
Journal Article
Hereditary Cancer in Clinical Practice, ISSN 1731-2302, 06/2013, Volume 11, Issue 1, pp. 4 - 4
Journal Article
Journal Article
Familial Cancer, ISSN 1389-9600, 1/2018, Volume 17, Issue 1, pp. 87 - 90
Journal Article
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 Medical Genetics Part A, ISSN 1552-4825, 01/2013, Volume 161, Issue 1, pp. 185 - 191
Dilation or aneurysm of the ascending aorta can progress to acute aortic dissection (Thoracic Aortic Aneurysms and Aortic Dissections, TAAD). Mutations in... 
SMAD4 | TGF‐beta signaling | thoracic aortic aneurysm and dissection | hereditary hemorrhagic telangiectasia | juvenile polyposis syndrome | aortic dilation | Aortic dilation | TGF-beta signaling | Hereditary hemorrhagic telangiectasia | Juvenile polyposis syndrome | Thoracic aortic aneurysm and dissection | PHENOTYPE | TGFBR2 MUTATIONS | BETA RECEPTOR | BMPR1A MUTATIONS | GENE | MARFAN-SYNDROME | MYHRE-SYNDROME | ANEURYSMS | GENETICS & HEREDITY | DISSECTIONS | Aortic Aneurysm, Thoracic - genetics | Receptors, Transforming Growth Factor beta - genetics | Humans | Male | Intestinal Polyposis - diagnosis | Telangiectasia, Hereditary Hemorrhagic - genetics | Smad3 Protein - genetics | Telangiectasia, Hereditary Hemorrhagic - diagnosis | Smad4 Protein - genetics | Aortic Aneurysm, Thoracic - diagnosis | Adult | Female | Aorta - physiopathology | Child | Microfilament Proteins - genetics | Telangiectasia, Hereditary Hemorrhagic - complications | Fibrillin-1 | Echocardiography | Signal Transduction | Intestinal Polyposis - genetics | Protein-Serine-Threonine Kinases - genetics | Fibrillins | Aortic Aneurysm, Thoracic - etiology | Marfan Syndrome - genetics | Transforming Growth Factor beta - genetics | Intestinal Polyposis - complications | Mutation | Telangiectasis | Children's hospitals | Genes | Medical genetics | Aneurysms | Bone morphogenetic proteins | Genetic aspects | Transforming growth factors | Cardiology | Marfan syndrome | Index Medicus | Aneurysm | juvenile polyposis Syndrome
Journal Article