Tags: Disease.
Weissenbacher–Zweymuller syndrome (WZS) also called Pierre-Robin syndrome with fetal chondrodysplasia is an autosomal recessive congenital disorder linked to mutations (955 gly -> glu) in the COL11A2 gene (located on chromosomal position 6p21.3) which codes for the α2 strand of collagen type XI. It is a collagenopathy types II and XI disorder.
