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https://rarediseases.info.nih.gov/diseases/3065/juvenile-polyposis-syndrome
57 rows · May 11, 2015 · Juvenile polyposis syndrome (JPS) is a disorder characterized by having a susceptibility to developing hamartomatous polyps in the gastrointestinal (GI) tract.. A hamartomatous polyp is a benign (noncancerous) tumor-like malformation made up of an abnormal mixture of cells and tissues.In JPS, these polyps can occur in the stomach, small intestine, colon, and rectum.
https://ghr.nlm.nih.gov/condition/juvenile-polyposis-syndrome
Oct 29, 2019 · Juvenile polyposis syndrome is a disorder characterized by multiple noncancerous (benign) growths called juvenile polyps. People with juvenile polyposis syndrome typically develop polyps before age 20; however, in the name of this condition "juvenile" refers to the characteristics of the tissues that make up the polyp, not the age of the affected individual.
https://www.chop.edu/conditions-diseases/juvenile-polyposis-syndrome
Juvenile polyposis syndrome is caused by alterations (also known as mutations) at specific areas within a person's genetic information. Each of us has a large amount of genetic information that is organized into smaller segments known as genes.
https://www.ncbi.nlm.nih.gov/books/NBK1469/
May 13, 2003 · Juvenile polyposis syndrome (JPS) is characterized by predisposition to hamartomatous polyps in the gastrointestinal (GI) tract, specifically in the stomach, small intestine, colon, and rectum. The term "juvenile" refers to the type of polyp rather than to the age of onset of polyps. Most individuals with JPS have some polyps by age 20 years; some may have only four or five polyps over their ...Cited by: 23
https://www.ncbi.nlm.nih.gov/pubmed/16246179
A review of juvenile polyposis syndrome. Chow E(1), Macrae F. Author information: (1)Department of Colorectal Medicine and Genetics, Royal Melbourne Hospital, Victoria, Australia. [email protected] Juvenile Polyposis Syndrome is an uncommon hamartomatous disorder with significant gastrointestinal malignant potential.Cited by: 137
https://www.cancertherapyadvisor.com/home/decision-support-in-medicine/pediatrics/gastrointestinal-polyps-juvenile-polyposis-jp/
Juvenile polyposis is a rare autosomal dominant condition characterized by multiple juvenile polyps primarily in the colorectum but can also be found throughout the upper gastrointestinal tract.Author: Carol Durno
https://www.uptodate.com/contents/juvenile-polyposis-syndrome
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https://www.hcctakesguts.org/peer-support
Hereditary Mixed Polyposis, Juvenile Polyposis Syndrome, Lynch Syndrome, Muir-Torre Syndrome, MYH-Associated Polyposis, Peutz-Jeghers Syndrome, Turcot Syndrome Below you will find support organizations, patient forums, and Facebook pages created by individuals who have been affected by hereditary colon cancer syndromes.
https://my.clevelandclinic.org/health/diseases/15221-juvenile-polyposis-syndrome-jps/resources
Juvenile Polyposis Syndrome (JPS) Menu. Overview Diagnosis and Tests Management and Treatment Prevention Outlook / Prognosis Living With Resources. ... Advertising on our site helps support our mission. We do not endorse non-Cleveland Clinic products or …
https://my.clevelandclinic.org/health/diseases/15221-juvenile-polyposis-syndrome-jps/management-and-treatment
How is juvenile polyposis syndrome (JPS) treated? There are no medicines to treat JPS. If there are just a few polyps, they can be removed during an endoscopic examination. To relieve symptoms, or if a large number of polyps are present, part of the stomach and intestine might need to be removed.
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