Pfeiffer syndrome

Pfeiffer syndrome (also known as type V acrocephalosyndactyly) is characterized by skull and limb abnormalities.

It affects about 1 in 100,000 births

Pfeiffer syndrome is strongly associated with mutations of the fibroblast growth factor receptor 1 gene (FGFR1) on chromosome 8 or the fibroblast growth factor receptor 2 (FGFR2) gene on chromosome 10.

  • type 1: classic Pfeiffer; most individuals have normal intelligence and lifespan. Inherited in an autosomal dominant pattern.
  • type 2: includes a cloverleaf skull (Kleeblattschädel); occurs sporadically and has a poor prognosis with severe neurological compromise.
  • type 3: includes craniosynostosis and severe proptosis; occurs sporadically and has poor prognosis.

It was first described by Rudolph Arthur Pfeiffer in 1964.

Consider other forms of acrocephalosyndactyly such as

Article information

rID: 68891
System: Paediatrics
Section: Syndromes
Synonyms or Alternate Spellings:
  • Pfeiffer's syndrome
  • Type V acrocephalosyndactyly

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Cases and figures

  • Case 1
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  • Case 2
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