Cerebro-costo-mandibular syndrome is a very rare genetic disorder which is characterized by jaw/chin, palate and rib abnormalities.
[1] The following list comprises the most common symptoms people with this disorder exhibit:[2] Common (but not the most) symptoms include: Not common but also not rare symptoms include: This disorder is caused by autosomal dominant mutations in the SNRPB gene, in chromosome 20.
[3] Only 110 cases have been described in medical literature.
[4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20]