Oromandibular-Limb Hypogenesis Syndrome

Oromandibular-Limb Hypogenesis Syndrome, also known as oroacral syndrome, is related to glossopalatine ankylosis and oroacral syndrome, verloes-koulischer type. Affiliated tissues include bone. (Oromandibular-Limb Hypogenesis Syndrome, also known as oroacral syndrome, is a genetic disorder characterized by abnormalities in the development of the jaw, mouth, and limbs. It is caused by mutations in the P63 gene, which is involved in the formation of bone and other tissues. The condition is also known as glossopalatine ankylosis and oroacral syndrome, verloes-koulischer type. It is inherited in an autosomal dominant pattern, which means that a person only needs to inherit one copy of the mutated gene from one parent to develop the condition. Affiliated tissues include bone.)