"Septo-Optic Dysplasia" 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 condition resulting from congenital malformations involving the brain. The syndrome of septo-optic dysplasia combines hypoplasia or agenesis of the SEPTUM PELLUCIDUM and the OPTIC NERVE. The extent of the abnormalities can vary. Septo-optic dysplasia is often associated with abnormalities of the hypothalamic and other diencephalic structures, and HYPOPITUITARISM.
    
			
			
				
				
					
						| Descriptor ID | D025962 | 
					
						| MeSH Number(s) | C10.500.840 C16.131.666.845 | 
					
						| Concept/Terms | Septo-Optic DysplasiaSepto-Optic DysplasiaSepto-Optic Dysplasia with Growth Hormone DeficiencySepto Optic Dysplasia with Growth Hormone DeficiencyDe Morsier SyndromeSyndrome, De MorsierSeptooptic DysplasiaDysplasia, SeptoopticDysplasias, SeptoopticSeptooptic Dysplasias
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				Below are MeSH descriptors whose meaning is more general than "Septo-Optic Dysplasia".
				
			 
			
			
				Below are MeSH descriptors whose meaning is more specific than "Septo-Optic Dysplasia".
				
			 
		 
	 
 
                                        
                                            
	
	
		
			
			
					
				This graph shows the total number of publications written about "Septo-Optic Dysplasia" by people in this website by year, and whether "Septo-Optic Dysplasia" was a major or minor topic of these publications. 
				
					 
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		            | Year | Major Topic | Minor Topic | Total | 
|---|
| 2021 | 2 | 0 | 2 | 
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				Below are the most recent publications written about "Septo-Optic Dysplasia" by people in Profiles.
						
					
								- 
								Bosch-Boonstra-Schaaf optic atrophy syndrome mimicking septo-optic dysplasia in a 10-year-old child. J AAPOS. 2021 10; 25(5):314-316. 
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								Prenatal diagnosis of middle interhemispheric variant of holoprosencephaly: Report of two cases. J Clin Ultrasound. 2021 Sep; 49(7):765-769.