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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:
-
Hydrogel
:
1 outcome 1 study in 1 result
: IBA
-
Type 2 Fibroblast Growth Factor Receptor (Fibroblast Growth Factor Receptor 2)
:
3 studies in 49 results
: IBA
-
tranilast (N 5')
:
1 study in 3 results
: IBA
-
Glycosaminoglycans
:
1 study in 2 results
: IBA
-
Frontonasal dysplasia
:
1 study in 2 results
: IBA
-
Silicones
:
1 study in 1 result
: IBA
-
Polyglycolic Acid (Polyglycolide)
:
1 study in 1 result
: IBA
-
poly(lactide) (polylactide)
:
1 study in 1 result
: IBA
-
Fibroblast Growth Factor Receptors (Fibroblast Growth Factor Receptor)
:
25 results
: IBA
-
Transcription Factors (Transcription Factor)
:
19 results
: IBA
Show All >>
Diseases Related to Acrocephalosyndactylia
-
Craniofacial Dysostosis (Crouzon Disease)
-
Craniosynostoses (Craniosynostosis)
-
Synostosis
-
Neoplasms (Cancer)
-
Acrocephalosyndactylia (Apert Syndrome)
Show All >>
Key Therapies for Acrocephalosyndactylia
Efficacy Chart >>
-
Sutures (Suture)
:
2 studies in 38 results
-
Distraction Osteogenesis
:
1 study in 13 results
-
Spinal Fusion (Spondylosyndesis)
:
1 study in 1 result
-
Hearing Aids (Hearing Aid)
:
1 study in 1 result
-
Osteotomy
:
13 results
Show All >>
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