Human L-Ficolin (Ficolin-2) and Its Clinical Significance

Table 3

Some disease associations of L-ficolin insufficiency.

Disease	Associated with	Reference
Perinatal infections	Low serum L-ficolin	[60]
Staphylococcal peritonitis	FCN2 +6359 variant allele (FCN2-B)	[65]
Bacterial infections following liver transplantation	FCN2 +6359 variant allele (FCN2-B)	[68]
Childhood infections combined with allergic diseases	Low serum L-ficolin	[62, 70]
Idiopathic bronchiectasis	Low serum L-ficolin	[73, 74]
Preeclampsia	Low serum L-ficolin	[63]
Chronic rheumatic heart disease	Promoter haplotype GGA	[79]