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Pfeiffer Syndrome


Research Notes on Pfeiffer Syndrome

Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of the sutures of the skull and deformity of the skull, preventing the skull from growing normally, which affects the normal growth of the face and head. Pfeiffer syndrome also affects the growth in the hands and feet.

Fast Facts:

  • Pfeiffer syndrome affects about 1 in 100,000 individuals.
  • More than half of all children with Pfeiffer syndrome have hearing loss and dental problems.
  • Types 2 and 3 are more severe forms of Pfeiffer syndrome.
  • The singer Prince had a son with Pfeiffer syndrome type 2, who died shortly after birth.

5 Great Resources on Pfeiffer Syndrome

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What is Pfeiffer Syndrome?

What Are The Symptoms of Pfeiffer Syndrome?

What Are The Causes and Complications of Pfeiffer Syndrome?

What Are The Treatments and Medications for Pfeiffer Syndrome?

What Are The Types, Diagnosis and Survival Rates of Pfeiffer Syndrome?

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Clinical Trials on Pfeiffer Syndrome

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About this WisdomCard

  • Contributor: Kathy
  • Reviewer: Nicole Kinsey
  • Supervised by: The OrganizedWisdom Physician Review Team
  • Redirects:Feiffer Syndrome, Pfeiffer Syndrom, Pfeifer Syndrome, Pfeeffer Syndrome, Pfeiffer syndrome, Pfeiffers Syndrome, Pfeiffer Syndromes, Pfeiffer Sindrome, Pfiffer Syndrome, Pfeiffer syndrome symptoms, What is pfeiffer syndrome, Pfeiffer syndrome treatments, Pfeiffer syndrome types, Pfeiffer syndrome support groups, Pfeiffer syndrome blogs, Pfeiffer syndrome message boards, Pfeiffer syndrome foundations, Pfeiffer syndrome clinical trials
  • Last update: Oct. 2, 2008

Each WisdomCard is handcrafted by our team of physician-guided health advocates. Our goal is to make it easy for you to find the most useful health resources for any health topic by filtering out spam and bad links.