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About 749 results

ALLMedicine™ Apert Syndrome Center

Research & Reviews  373 results

Maxillary Changes Following Facial Bipartition - A Three-Dimensional Quantification.
https://doi.org/10.1097/SCS.0000000000007632
The Journal of Craniofacial Surgery; Rickart AJ, van de Lande LS et. al.

Mar 26th, 2021 - Children with Apert syndrome have hypertelorism and midfacial hypoplasia, which can be treated with facial bipartition (FB), often aided by rigid external distraction. The technique involves a midline osteotomy that lateralizes the maxillary segme...

Satisfying Clinical and Functional Results in 12 Apert Children Treated With Soft Tissu...
https://doi.org/10.1097/BPO.0000000000001785
Journal of Pediatric Orthopedics; Winge MI, Røkkum M

Mar 12th, 2021 - The complex syndactyly in Apert syndrome hands is challenging to operate. The synostosis and tightness of skin between third and fourth digits lead to severe coverage problems during ray release. A soft tissue distractor can simplify the release w...

Slide tracheoplasty for tracheal cartilaginous sleeve in a patient with Apert syndrome.
https://doi.org/10.1016/j.athoracsur.2021.02.048
The Annals of Thoracic Surgery; Darr OA, Stone ML et. al.

Mar 7th, 2021 - Apert syndrome is a form of acrocephalosyndactyly involving craniosynostosis, syndactyly, and less commonly tracheal cartilaginous sleeve (TCS), a potential cause of tracheal stenosis. Slide tracheoplasty is performed in children with tracheal ste...

Is the Apert foot an overlooked aspect of this rare genetic disease? Clinical findings ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700708
BMC Musculoskeletal Disorders; Stauffer A, Farr S

Nov 29th, 2020 - Apert syndrome is characterised by the presence of craniosynostosis, midface retrusion and syndactyly of hands and feet, thus, synonymously referred to as acrocephalosyndactyly type I. Considering these multidisciplinary issues, frequently requiri...

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Guidelines  1 results

FACES Guideline: What is Apert Syndrome?
http://docs.wixstatic.com/ugd/1e6e01_646faee57b9242dca896ad6deb4daca7.pdf
The National Craniofacial Association

Feb 11th, 2016 - Description of Apert Syndrome aimed at helping parents understand the syndrome and the surgeries that may be required. Provides list of additional resources.

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Clinicaltrials.gov  375 results

Maxillary Changes Following Facial Bipartition - A Three-Dimensional Quantification.
https://doi.org/10.1097/SCS.0000000000007632
The Journal of Craniofacial Surgery; Rickart AJ, van de Lande LS et. al.

Mar 26th, 2021 - Children with Apert syndrome have hypertelorism and midfacial hypoplasia, which can be treated with facial bipartition (FB), often aided by rigid external distraction. The technique involves a midline osteotomy that lateralizes the maxillary segme...

Satisfying Clinical and Functional Results in 12 Apert Children Treated With Soft Tissu...
https://doi.org/10.1097/BPO.0000000000001785
Journal of Pediatric Orthopedics; Winge MI, Røkkum M

Mar 12th, 2021 - The complex syndactyly in Apert syndrome hands is challenging to operate. The synostosis and tightness of skin between third and fourth digits lead to severe coverage problems during ray release. A soft tissue distractor can simplify the release w...

Slide tracheoplasty for tracheal cartilaginous sleeve in a patient with Apert syndrome.
https://doi.org/10.1016/j.athoracsur.2021.02.048
The Annals of Thoracic Surgery; Darr OA, Stone ML et. al.

Mar 7th, 2021 - Apert syndrome is a form of acrocephalosyndactyly involving craniosynostosis, syndactyly, and less commonly tracheal cartilaginous sleeve (TCS), a potential cause of tracheal stenosis. Slide tracheoplasty is performed in children with tracheal ste...

Is the Apert foot an overlooked aspect of this rare genetic disease? Clinical findings ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700708
BMC Musculoskeletal Disorders; Stauffer A, Farr S

Nov 29th, 2020 - Apert syndrome is characterised by the presence of craniosynostosis, midface retrusion and syndactyly of hands and feet, thus, synonymously referred to as acrocephalosyndactyly type I. Considering these multidisciplinary issues, frequently requiri...

see more →