Conditions

Genetic condition characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face.

Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain skull bones (craniosynostosis). This early fusion prevents the skull from growing normally and affects the shape of the head and face. Pfeiffer syndrome also affects bones in the hands and feet.

Robin sequence or Pierre Robin syndrome begins with a lower jaw that is either too small (micrognathia) or is set back from the upper jaw (retrognathia).

Children with microtia do not hear well and have ears that may look abnormal. The outer, visible portion of the ear (the pinna or auricle) is underdeveloped.

A very rare condition, also known as Miller or Wildervanck-Smith syndrome, with characteristics that include underdeveloped cheekbones, an abnormally small jaw, a cleft palate, small, protruding "cup-shaped" ears, and drooping of the lower eyelids.

Nager syndrome is a rare condition that mainly affects the development of the face, hands, and arms. Children with Nager syndrome are born with underdeveloped cheek bones (malar hypoplasia) and a very small lower jaw (micrognathia)

Treacher Collins syndrome is an autosomal dominant congenital disorder characterized by craniofacial deformities, typically involving the ears, eyes, cheekbones, and jawbone.

Form of craniosynostosis results from a premature fusion between the two bones of the forehead. Children with this condition tend to have a triangular or keel-shaped forehead.

Möbius syndrome is an extremely rare congenital neurological disorder which is characterized by facial paralysis and the inability to move the eyes from side to side.

Lymphatic malformation (LM) is an abnormality of lymph vessels.