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