Related Conditions and Treatments
Apert Syndrome
Condition
Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones.
Beckwith-Wiedemann Syndrome
Condition
Beckwith-Wiedemann syndrome is a genetic disorder that can cause an overgrowth of particular body parts.
Binder Syndrome
Condition
Binder syndrome is a congenital condition that causes an underdeveloped midface and nose.
Bone-Anchored Hearing Systems
Treatment
Bone-anchored hearing systems (BAHS) are devices used to treat ear conditions that interfere with hearing.
Craniosynostosis
Condition
Craniosynostosis is a condition in which the fibrous connections grow together (fuse) too early.
Crouzon Syndrome
Condition
Crouzon syndrome is a complex genetic birth disorder that may affect a child’s face, skull, and teeth.
Encephaloceles
Condition
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.
Endoscopic Strip Craniectomy
Treatment
Endoscopic strip craniectomy is a minimally invasive procedure to treat craniosynostosis.
Hemifacial Microsomia
Condition
Hemifacial microsomia is a condition in which half of one side of the face is underdeveloped and doesn't grow normally.
Oromandibular Limb Hypoplasia
Condition
Oromandibular limb hypoplasia is a group of rare conditions that involve congenital malformations of the tongue and jawbones.
Treacher Collins Syndrome
Condition
Treacher Collins syndrome is a genetic birth disorder characterized by the premature joining of certain bones of the skull during development.