"Peutz-Jeghers Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, 
	MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, 
	which enables searching at various levels of specificity.
	
	
		
			
			
				A hereditary disease caused by autosomal dominant mutations involving CHROMOSOME 19. It is characterized by the presence of INTESTINAL POLYPS, consistently in the JEJUNUM, and mucocutaneous pigmentation with MELANIN spots of the lips, buccal MUCOSA, and digits.
    
			
			
				
				
					
						| Descriptor ID | D010580 | 
					
						| MeSH Number(s) | C04.700.705 C06.405.469.578.750 C16.320.700.705 C17.800.621.430.530.550.625 | 
					
						| Concept/Terms | Peutz-Jeghers SyndromePeutz-Jeghers SyndromePeutz Jeghers SyndromeSyndrome, Peutz-JeghersPolyposis, Hamartomatous IntestinalHamartomatous Intestinal PolyposesHamartomatous Intestinal PolyposisIntestinal Polyposes, HamartomatousIntestinal Polyposis, HamartomatousPolyposes, Hamartomatous IntestinalPeutz-Jegher's SyndromePeutz Jegher's SyndromePeutz-Jegher SyndromeSyndrome, Peutz-Jegher'sPeutz-Jeghers PolyposisPeutz Jeghers PolyposisPolyposis, Peutz-JeghersPeriorificial Lentiginosis SyndromePeriorificial Lentiginosis SyndromesSyndrome, Periorificial LentiginosisSyndromes, Periorificial LentiginosisLentiginosis, PerioralLentiginoses, PerioralPerioral LentiginosesPerioral LentiginosisPolyps-and-Spots SyndromePolyps and Spots SyndromePolyps-and-Spots SyndromesSyndrome, Polyps-and-SpotsSyndromes, Polyps-and-Spots
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				Below are MeSH descriptors whose meaning is more general than "Peutz-Jeghers Syndrome".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Peutz-Jeghers Syndrome".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Peutz-Jeghers Syndrome" by people in this website by year, and whether "Peutz-Jeghers Syndrome" was a major or minor topic of these publications. 
				
					 
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		            | Year | Major Topic | Minor Topic | Total | 
|---|
| 2003 | 0 | 1 | 1 | 
| 2005 | 1 | 0 | 1 | 
| 2007 | 0 | 1 | 1 | 
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				Below are the most recent publications written about "Peutz-Jeghers Syndrome" by people in Profiles.
						
					
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								Interobserver agreement for EUS findings in familial pancreatic-cancer kindreds. Gastrointest Endosc. 2007 Jul; 66(1):62-7. 
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								Gynecomastia and mucosal lentigines in an 8-year-old boy. J Am Acad Dermatol. 2005 Oct; 53(4):660-2. 
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								Restoration of silenced Peutz-Jeghers syndrome gene, LKB1, induces apoptosis in pancreatic carcinoma cells. Neoplasia. 2003 Jul-Aug; 5(4):367-74.