ALG8 and congenital disorder of glycosylation: ALG8-CDG is a CDG form with dysmorphism (retrognathia, low-set ears, pes equinovarus), muscular hypotonia, hepatomegaly, coagulopathy (thrombocytopenia), edema and ascites (including fetal hydrops), cardiorespiratory problems, and protein-losing enteropathy (watery diarrhea) [8].