Clinical features and genetic characteristics of primary immunodeficiency disease with skin symptoms in 15 children
	    		
		   		
		   			
		   		
	    	
    	 
    	10.3969/j.issn.1000-3606.2018.01.005
   		
        
        	
        		- VernacularTitle:伴皮肤症状原发性免疫缺陷病15例临床特征及基因分析
 
        	
        	
        	
        		- Author:
	        		
		        		
		        		
			        		Tingyan HE
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Yanyan HUANG
			        		
			        		;
		        		
		        		
		        		
			        		Zhongxiang QI
			        		
			        		;
		        		
		        		
		        		
			        		Xianze LUO
			        		
			        		;
		        		
		        		
		        		
			        		Jun YANG
			        		
			        		
		        		
		        		
		        		
		        		
		        			
			        		
			        		Author Information
			        		
		        		
		        		
			        		
			        		
			        			1. 深圳市儿童医院风湿免疫科 广东深圳 518038
			        		
		        		
	        		
        		 
        	
        	
        	
        	
        		- Keywords:
        			
	        			
	        				
	        				
			        		
				        		immunodeficiency disease;
			        		
			        		
			        		
				        		skin symptoms;
			        		
			        		
			        		
				        		recurrent infection;
			        		
			        		
			        		
				        		autoimmunity;
			        		
			        		
			        		
				        		autoinflammation
			        		
			        		
	        			
        			
        		
 
        	
            
            
            	- From:
	            		
	            			Journal of Clinical Pediatrics
	            		
	            		 2018;36(1):19-24
	            	
            	
 
            
            
            	- CountryChina
 
            
            
            	- Language:Chinese
 
            
            
            	- 
		        	Abstract:
			       	
			       		
				        
				        	Objective To explore the clinical features and genetic characteristics of primary immunodeficiency disease (PIDs) with skin symptoms in children. Methods The clinical data of PIDs with skin symptoms in 15 children from January 2014 to March 2017 were analyzed retrospectively. Results The median age at onset in 15 children was 4 months (neonatal period to 11 years 8 months). All of them showed obvious skin symptoms, including eczema or chilblain rash, pustular psoriasis, skin infections, subcutaneous hemorrhage or skin ecchymosis, ichthyosiform erythroderma, progeroid appearance, or other cutaneous vasculitis. The accompanying manifeslations included recurrent infections, auto inflammation, autoimmunity, growth retardation, or lymphoid proliferation, and impairment of brain, lung, kidney and other important organs. Eosinophil counts were increased in 5 children, IgE levels were elevated in 5 children, and 4 children were abnormal in both indicators. Gene detection showed WAS, RNASEH2C, NLRP12, IL36RN, NRAS, PIK3CD, STAT1, FOXP3, STAT3, DOCK8, TYK2, SPINK5, NBAS or ITGB2 gene mutations, respectively. Two children died from multiple organ dysfunction syndrome, 1 child was lost for follow up, the remaining 12 children survived and were under the individualized treatment. Conclusions A variety of PIDs can have skin symptoms. When accompanied by recurrent infections, auto inflammation, autoimmune, growth retardation, or lymph proliferation, PIDs should be considered, and gene detection is helpful for the diagnosis.