Cerebro-costo-mandibular syndrome is a very rare genetic disorder which is characterized by jaw/chin, palate and rib abnormalities.
The following list comprises the most common symptoms people with this disorder exhibit:
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.
Only 110 cases have been described in medical literature.