"Romano-Ward 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 form of long QT syndrome that is without congenital deafness. It is caused by mutation of the KCNQ1 gene which encodes a protein in the VOLTAGE-GATED POTASSIUM CHANNEL.
    
			
			
				
				
					
						| Descriptor ID | D029597 | 
					
						| MeSH Number(s) | C14.280.067.565.720 C14.280.123.625.720 C16.131.240.400.715.720 C23.550.073.547.720 | 
					
						| Concept/Terms | Romano-Ward SyndromeRomano-Ward SyndromeRomano Ward SyndromeSyndrome, Romano-WardVentricular Fibrillation with Prolonged QT IntervalLong QT Syndrome Type 1Long QT Syndrome 1Ward-Romano SyndromeSyndrome, Ward-RomanoWard Romano Syndrome
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				Below are MeSH descriptors whose meaning is more general than "Romano-Ward Syndrome".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Romano-Ward Syndrome".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Romano-Ward Syndrome" by people in this website by year, and whether "Romano-Ward Syndrome" was a major or minor topic of these publications. 
				
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				Below are the most recent publications written about "Romano-Ward Syndrome" by people in Profiles.