Congenital Disorder of Glycosylation, Type Iic (CDG2C)

Congenital Disorder of Glycosylation, Type Iic, also known as leukocyte adhesion deficiency type ii, is related to rapp-hodgkin syndrome and herpes zoster oticus, and has symptoms including seizures An important gene associated with Congenital Disorder of Glycosylation, Type Iic is SLC35C1 (Solute Carrier Family 35 Member C1), and among its related pathways/superpathways is Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell. Affiliated tissues include neutrophil and eye, and related phenotypes are failure to thrive and coarse facial features