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

Genotype-Phenotype Correlation in Fibrous Dysplasia/McCune-Albright Syndrome Patients With Craniofacial Lesions.

Oral diseases - 1 Jan 2026

Xue Jiang, Li Xuefen, Feng Yanrui, Sun Lisha, Li Tiejun

Abstract excerpt

OBJECTIVES: We aimed to investigate genotype-phenotype correlations, variant prevalence, and prognostic factors in a Chinese cohort with craniofacial FD/MAS. METHODS: A retrospective study of 93 histologically confirmed FD/MAS cases (2003-2024) analyzed GNAS mutations via direct sequencing. Clinical data, including disease onset, lesion activity (active vs. stable), and extraskeletal manifestations, were...

Read the complete abstract on PubMed

Topics

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

Share to Child, Preschool
Share to China
Share to Chromogranins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fibrous Dysplasia, Polyostotic

Share to Genetic Association Studies

Share to GTP-Binding Protein alpha Subunits, Gs

Share to Prognosis

Share to Young Adult

Source

Identifiers

PMID: 40887809
DOI: 10.1111/odi.70074

Genes

GNAS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotype-Phenotype Correlation in Fibrous Dysplasia/McCune-Albright Syndrome Patients With Craniofacial Lesions.PMID 40887809Read ↗

Genotype-Phenotype Correlation in Fibrous Dysplasia/McCune-Albright Syndrome.Semantic proximity Read ↗

Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohort.Semantic proximity Read ↗

Multidisciplinary approach and clinical management of McCune-Albright syndrome.Semantic proximity Read ↗

The Clinical Spectrum of McCune-Albright Syndrome and Its Management.Semantic proximity Read ↗

Fibrous Dysplasia/McCune-Albright Syndrome: Clinical and Translational PerspectivesSemantic proximity Read ↗

Clinicopathological and genetic study of a rare occurrence: Malignant transformation of fibrous dysplasia of the jawsSemantic proximity Read ↗

Whole Exome Sequencing as an Effective Molecular Diagnosis Tool for Craniofacial Fibrous Dysplasia with Ocular Complications.Semantic proximity Read ↗

Exploring mutations: GNAS and CDC73 in jaw fibroosseous lesions.Semantic proximity Read ↗

Fibrous Dysplasia/McCune-Albright Syndrome: A Rare, Mosaic Disease of Gα s ActivationSemantic proximity Read ↗

Fibrous dysplasia of the jaws: Integrating molecular pathogenesis with clinical, radiological, and histopathological featuresSemantic proximity Read ↗

Gorlin Syndrome: Assessing Genotype-Phenotype Correlations and Analysis of Early Clinical Characteristics as Risk Factors for Disease SeveritySemantic proximity Read ↗

G(s)alpha mutations in fibrous dysplasia and McCune-Albright syndrome.Semantic proximity Read ↗

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