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Dictionary » Pfeiffer syndrome

Pfeiffer syndrome

Introduction: Pfeiffer syndrome

Description of Pfeiffer syndrome

Pfeiffer syndrome (medical condition): A rare genetic disorder where some of the skull bones fuse too early...more »

See also:

Pfeiffer syndrome:
  »Introduction: Pfeiffer syndrome
  »Symptoms of Pfeiffer syndrome

Pfeiffer syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Pfeiffer syndrome:

Pfeiffer syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Pfeiffer syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Pfeiffer syndrome, or a subtype of Pfeiffer syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)


Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Pfeiffer syndrome as a "rare disease".

Source - Orphanet

Pfeiffer syndrome as a Disease

Pfeiffer syndrome (medical condition): See Pfeiffer syndrome (disease information).
  »Introduction: Pfeiffer syndrome
  »Symptoms of Pfeiffer syndrome

Pfeiffer syndrome: Related Diseases

Pfeiffer syndrome: Pfeiffer syndrome is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Pfeiffer syndrome:

Pfeiffer syndrome: Related Disease Topics

These medical disease topics may be related to Pfeiffer syndrome:

Terms associated with Pfeiffer syndrome:

Terms Similar to Pfeiffer syndrome:

Source: Diseases Database

Source - NIH

External links related to: Pfeiffer syndrome

Source: Diseases Database

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