Medicine:Cardiocranial syndrome, Pfeiffer type

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Cardiocranial syndrome, Pfeiffer type
Other namesCardiocranial syndrome
Craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis
Pfeiffer Singer Zschiesche syndrome

Cardiocranial syndrome, Pfeiffer type is a rare multiple disorder syndrome characterized by congenital heart defects, sagittal craniosynostosis, and severe developmental delay. The condition has been reported in less than 10 patients worldwide.[1][2][3][4]

Signs and symptoms

Features of this condition include:[1][2]

  • Abnormal heart morphology
  • Abnormality of cardiovascular system morphology
  • Aplasia uvulae
  • Cleft palate
  • Cryptorchidism
  • Hypertelorism
  • Low-set, dysplastic ears
  • Micropenis
  • Micrognathia (or retrognathia)
  • Sagittal craniosynostosis
  • Strabismus
  • Trismus
  • Intellectual disability
  • Abnormal tracheobronchial morphology
  • Growth delay

Symptoms also reported include large joint contractures, syndactyly, rib anomalies and hypoplastic kidneys; a few cases did not show cardiac anomalies.[2]

Causes

The condition is genetic but its origins are unclear. The condition has been seen in brother-sister sibling pairs, suggesting autosomal recessive inheritance, however autosomal dominant inheritance and submicroscopic deletions (not inherited) have been suggested.[1]

References