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Jul 25, 2023 · Pfeiffer syndrome is a rare genetic disorder characterized by premature fusion of certain skull bones (craniosynostosis) and broad and medially deviated thumbs and great toes. Most affected individuals also have differences to their midface (protruding eyes) and conductive hearing loss.
Sep 28, 2017 · Overview. Pfeiffer syndrome happens when the bones in your child’s skull, hands, and feet have fused together too soon in the womb because of a gene mutation. This can cause physical,...
Description. 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.
Summary. Pfeiffer syndrome is a disorder that affects the development of the bones in the skull, hands and feet. Signs and symptoms can include craniosynostosis, which prevents normal skull growth and affects the shape of the head and face; distinctive facial features including bulging and wide-set eyes, a high forehead, an underdeveloped upper ...
Mar 22, 2024 · 8 min read. What Is Pfeiffer Syndrome? Pfeiffer syndrome is a rare birth condition that affects the shape of a baby’s skull and face. When you’re born, the top of your...
Pfeiffer syndrome is a complex genetic disorder that affects your child’s head, face, hands, and feet. Clinical features vary for different children and range from mild to severe. Pfeiffer syndrome may include:
Jul 14, 2023 · Pfeiffer syndrome is a rare genetic condition that causes the premature fusing of the skull, resulting in an abnormal shaping of the face and head. It also affects the hands and feet. The cause...
