Related Conditions and Treatments
Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones.
Beckwith-Wiedemann syndrome is a genetic disorder that can cause an overgrowth of particular body parts.
Binder syndrome is a congenital condition that causes an underdeveloped midface and nose.
Craniosynostosis is a condition in which the fibrous connections grow together (fuse) too early.
Crouzon syndrome is a complex genetic birth disorder that may affect a child’s face, skull, and teeth.
An encephalocele is a rare birth defect in which the tissue covering the brain, and a portion of the brain itself, protrude through openings in the skull.
Hemifacial microsomia is a condition in which half of one side of the face is underdeveloped and doesn't grow normally.
Oromandibular Limb Hypoplasia
Oromandibular limb hypoplasia is a group of rare conditions that involve congenital malformations of the tongue and jawbones.
Treacher Collins Syndrome
Treacher Collins syndrome is a genetic birth disorder characterized by the premature joining of certain bones of the skull during development.