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

Cleft palate in Pfeiffer syndrome.

The Journal of craniofacial surgery - 1 Sept 2009

Stoler Joan M, Rosen Heather, Desai Urmen, Mulliken John B, Meara John G, Rogers Gary F

Abstract excerpt

The frequency of associated cleft palate is known to be high in some fibroblast growth factor receptor 2 (FGFR2)-mediated craniosynostosis syndromes, such as Apert syndrome. However, there is little information on the frequency of palatal clefts in the FGFR2-mediated disorder, that is, Pfeiffer syndrome. The purpose of this study was to determine the frequency of palatal clefts in patients with Pfeiffer syndrome....

Read the complete abstract on PubMed

Topics

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

Share to Acrocephalosyndactylia
Share to Boston
Share to Cleft Palate

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Mutation

Share to Palate

Share to Receptor, Fibroblast Growth Factor, Type 1

Share to Receptor, Fibroblast Growth Factor, Type 2

Source

Identifiers

PMID: 19816260
DOI: 10.1097/SCS.0b013e3181ae42e4

Genes

FGFR2
FGFR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Cleft palate in Pfeiffer syndrome.PMID 19816260Read ↗

Feeding, Communication, Hydrocephalus, and Intracranial Hypertension in Patients With Severe FGFR2-Associated Pfeiffer Syndrome.Semantic proximity Read ↗

Pfeiffer syndrome.Semantic proximity Read ↗

Pfeiffer syndrome: analysis of a clinical series and development of a classification system.Semantic proximity Read ↗

Upper extremity anomalies in Pfeiffer syndrome and mutational correlations.Semantic proximity Read ↗

Familial Pfeiffer Syndrome: Variable Manifestations and Role of Multidisciplinary Team Care.Semantic proximity Read ↗

FGFR2 mutations in Pfeiffer syndrome.Semantic proximity Read ↗

Pfeiffer mutation in an Apert patient: how wide is the spectrum of variability due to mutations in the FGFR2 gene?Semantic proximity Read ↗

Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.Semantic proximity Read ↗

FGFR1 and FGFR2 mutations in Pfeiffer syndrome.Semantic proximity Read ↗

Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome.Semantic proximity Read ↗

Variable expressivity and clinical heterogeneity can complicate the diagnosis and management of Pfeiffer syndrome.Semantic proximity Read ↗

Audiologic findings in Pfeiffer syndrome.Semantic proximity Read ↗

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