Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Apert syndrome: evaluation of a treatment algorithm.

Plastic and reconstructive surgery - 1 Jan 2013

Fearon Jeffrey A, Podner Cindy

Abstract excerpt

BACKGROUND: The authors catalogued phenotypic variability among children with Apert syndrome, reviewed surgical outcomes (particularly with respect to their treatment goals of avoiding preventable developmental delays and reducing operative interventions), and examined correlations that might stimulate improved treatment paradigms. METHODS: A case series review of all Apert syndrome patients, treated by a single...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acrocephalosyndactylia
Share to Algorithms
Share to Decision Support Techniques

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Developmental Disabilities

Share to Genetic Markers

Share to Receptor, Fibroblast Growth Factor, Type 2

Share to Reoperation

Share to Treatment Outcome

Source

Identifiers

PMID: 23271523
DOI: 10.1097/PRS.0b013e3182729f42

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Apert syndrome: evaluation of a treatment algorithm.PMID 23271523Read ↗

Prenatal diagnosis and management of Apert syndrome in a low-middle income country: Case reportSemantic proximity Read ↗

Apert syndrome.Semantic proximity Read ↗

Atypical presentation of a newborn with Apert syndrome.Semantic proximity Read ↗

Apert syndrome: what prenatal radiographic findings should prompt its consideration?Semantic proximity Read ↗

The spectrum of Apert syndrome: phenotype, particularities in orthodontic treatment, and characteristics of orthognathic surgery.Semantic proximity Read ↗

[Apert syndrome or acrocephalosyndactilia type I].Semantic proximity Read ↗

Prenatal diagnosis of Apert syndrome.Semantic proximity Read ↗

[Apert syndrome: clinico-epidemiological analysis of a series of consecutive cases in Spain].Semantic proximity Read ↗

Craniosynostosis: Acrocephalosyndactyly (Apert Syndrome) Diagnosed in a Newborn.Semantic proximity Read ↗

FGFR2 gene Related Apert and Crouzon Syndrome Patients with Different Craniofacial Dysmorphisms: A Systematic Review and Meta-analysisSemantic proximity Read ↗

Monobloc minus Le Fort II for single-stage treatment of the Apert phenotype.Semantic proximity Read ↗

Craniosynostosis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.