Bird-face syndrome, also known as maxillofacial hypoplasia and deaf syndrome, is a congenital genetic disorder.
Bird’s face syndrome is usually caused by autosomal dominant inheritance or gene mutation. It is usually caused by abnormal development of the first and second gill arches in the early embryonic stage, and is accompanied by deafness and other conditions.
Symptoms often include a bird-like appearance, such as small eyes, a hawk-like nose, fleshy ears, drooping upper eyelids, and an inability to open the eye slits.
There is no good clinical treatment for Bird Face Syndrome, so it is recommended to consult a doctor in time and have orthopedic surgeries according to the patient’s different manifestations.