Autosomal Dominant Kenny-Caffey Syndrome

Autosomal Dominant Kenny-Caffey Syndrome is related to kenny-caffey syndrome, type 2 and gracile bone dysplasia. An important gene associated with Autosomal Dominant Kenny-Caffey Syndrome is FAM111A (FAM111 Trypsin Like Peptidase A). Affiliated tissues include bone and eye, and related phenotypes are short stature and delayed cranial suture closure