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Acrocephalosyndactylia (Apert Syndrome) Summary

Description: Congenital craniostenosis with syndactyly.

Also Known As: Apert Syndrome; Pfeiffer Syndrome; Saethre Chotzen Syndrome; Syndrome, Pfeiffer; Syndrome, Apert Show All >>

Networked: 259 relevant articles (1 outcomes, 14 trials/studies) for this Disease

Key Drugs and Agents for Acrocephalosyndactylia

Efficacy Chart >>
Drugs and Important Biological Agents (IBA) related to treatments:
  1. Hydrogel : 1 outcome 1 study in 1 result : IBA
  2. Type 2 Fibroblast Growth Factor Receptor (Fibroblast Growth Factor Receptor 2) : 3 studies in 49 results : IBA
  3. tranilast (N 5') : 1 study in 3 results : IBA
  4. Glycosaminoglycans : 1 study in 2 results : IBA
  5. Frontonasal dysplasia : 1 study in 2 results : IBA
  6. Silicones : 1 study in 1 result : IBA
  7. Polyglycolic Acid (Polyglycolide) : 1 study in 1 result : IBA
  8. poly(lactide) (polylactide) : 1 study in 1 result : IBA
  9. Fibroblast Growth Factor Receptors (Fibroblast Growth Factor Receptor) : 25 results : IBA
  10. Transcription Factors (Transcription Factor) : 19 results : IBA
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Diseases Related to Acrocephalosyndactylia

  1. Craniofacial Dysostosis (Crouzon Disease)
  2. Craniosynostoses (Craniosynostosis)
  3. Synostosis
  4. Neoplasms (Cancer)
  5. Acrocephalosyndactylia (Apert Syndrome)
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Key Therapies for Acrocephalosyndactylia

Efficacy Chart >>
  1. Sutures (Suture) : 2 studies in 38 results
  2. Distraction Osteogenesis : 1 study in 13 results
  3. Spinal Fusion (Spondylosyndesis) : 1 study in 1 result
  4. Hearing Aids (Hearing Aid) : 1 study in 1 result
  5. Osteotomy : 13 results
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