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Today's Terms
Apert syndrome
Definition:
Apert Syndrome is a genetic defect and falls under the broad classification of craniofacial/limb anomalies. It can be inherited from a parent who has Apert, or may be a fresh mutation. It occurs in approximately 1 per 160,000 to 200,000 live births. Apert syndrome is primarily characterized by specific malformations of the skull, midface, hands, and feet.
neural tube defect
Definition:
A structure in early fetal life that develops into the brain, spinal cord, spinal nerves and spine.
Bell's palsy
Definition:
A weakness or paralysis of the muscles that control expression on one side of the face because of damage to a facial nerve.
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