Disease: Microsomia hemifacial radial defects
- "I can't provide what my child needs": Early feeding experiences of caregivers of children with craniofacial microsomia
- 3D-CT measurements of facial symmetry in severe CFM patients: A comparative study between mandibular ascending ramus distraction osteogenesis and bone grafting
- A 3-Dimensional Evaluation of the Effects of Unilateral Vertical Mandibular Distraction Osteogenesis on Airway Volume Among Patients With Hemifacial Microsomia
- A 3-month-old male infant with Goldenhar syndrome: A clinical case report from Woldia, Northeast Ethiopia
- A case of 14q terminal deletion syndrome and hemifacial microsomia with review of terminal 14q deletion cases
- A case of Abernethy malformation type I combined with hepatoblastoma
- A clinical epidemiological study on congenital ear malformation (CEM)
- A missense mutation in the <em>C. elegans src-2</em> tyrosine-protein kinase reduces brood size and enhances embryonic morphogenesis defects in <em>src-1(RNAi)</em> conditions
- A missense mutation in the C. elegans src-2 tyrosine-protein kinase reduces brood size and enhances embryonic morphogenesis defects in src-1(RNAi) conditions
- Air Embolism-Induced Ischemic Stroke Following Orthognathic Surgery in a Patient With Goldenhar Syndrome
- An Atypical Presentation of Goldenhar Syndrome With Seizures: A Rare Case Report
- An updated protocol for mandibular reconstruction in nongrowing patients with craniofacial microsomia with temporomandibular joint total prosthesis
- Astigmatic reduction after dermoid excision in a child with Goldenhar syndrome
- Bilateral Maxillary Duplication in Tessier No. 7 Cleft: An Uncommon Congenital Deformity with a Challenging Radiological Diagnosis
- Bioinformatics Analysis of Hub Genes Involved in Smoke-Induced Hemifacial Microsomia Pathogenesis
- Bone Density of the Condyle of Children with Craniofacial Microsomia and its Correlation with Condylar Resorption After Mandible Distraction Osteogenesis
- Breaking the silence: A qualitative exploration of parental perspectives of children with Goldenhar Syndrome
- Caruncle dysgeneses - A case series
- Characterising the speech phenotype in individuals with craniofacial microsomia: a scoping review protocol
- Characterizing Speech Phenotype in Individuals With Craniofacial Microsomia: A Scoping Review
- Clinical and Genetic Correlation in Neurocristopathies: Bridging a Precision Medicine Gap
- Clinical report and genetic analysis of a Chinese neonate with craniofacial microsomia caused by a splicing variant of the splicing factor 3b subunit 2 gene
- Cochlear Implantation in Goldenhar Syndrome
- Commentary: Endoscopic Endonasal Odontoidectomy for Upper Cervical Spine and Brainstem Decompression in a Patient With Goldenhar Syndrome: 2-Dimensional Operative Video
- Complex Presentation of Goldenhar Syndrome in a Preterm Neonate: A Case Report
- Computed tomography assessment of hypodontia and crown size in hemifacial microsomia
- Concurrent Occurrence of Ear Tag With Posterior Talon Cusp, Fissured Tongue, and Ankyloglossia: A Case Report
- Condylar resorption post mandibular distraction osteogenesis in craniofacial microsomia: A retrospective study
- Craniocervical Instability in Oculoauriculovertebral Spectrum
- Craniofacial Microsomia, Associated Congenital Anomalies, and Risk Factors in 63 Cases from the Alberta Congenital Anomalies Surveillance System
- Craniofacial Microsomia: New Updates in Spinal Anomalies
- Cryptophthalmos: associated syndromes and genetic disorders
- CT features of abnormally whole-course wide eustachian tubes with microtia and atresia
- Dental manifestations of a paediatric patient with Goldenhar syndrome
- Diagnostic Imageology of Goldenhar Syndrome: Report of a Rare Case
- Discrepancy in Mandibular Medullary Cavity on Different Sides: More Hints Towards Understanding Hemifacial Microsomia
- Distribution and Phenotype of Goldenhar Syndrome and Its Association With Other Anomalies
- Early Experiences of Parents of Children With Craniofacial Microsomia
- Efficacy of navigation system-assisted distraction osteogenesis for hemifacial microsomia based on artificial intelligence for 3 to 18 years old: study protocol for a randomized controlled single-blind trial
- Endoscopic Endonasal Odontoidectomy for Upper Cervical Spine and Brainstem Decompression in a Patient With Goldenhar Syndrome: 2-Dimensional Operative Video
- Establishing an International Interdisciplinary Research Network in Craniofacial Microsomia: The CARE Program
- Evaluation of Research Diagnostic Criteria in Craniofacial Microsomia
- Expanding the Etiology of Oculo-Auriculo-Vertebral Spectrum: A Novel Interstitial Microdeletion at 1p36
- Exploration of Novel Genetic Evidence and Clinical Significance Into Hemifacial Microsomia Pathogenesis
- FBLN2 is associated with Goldenhar syndrome and is essential for cranial neural crest cell development
- Focuses, Trends, and Developments in Craniofacial Microsomia From 1992 to 2022: A Bibliometric Analysis
- FOXI3 pathogenic variants cause one form of craniofacial microsomia
- Functional and Genetic Analyses Unveil the Implication of CDC27 in Hemifacial Microsomia
- Goldenhar syndrome
- Goldenhar syndrome complicated with subglottic airway stenosis: a case report
- Goldenhar Syndrome Patient with Craniocerebral Lesion
- Goldenhar syndrome with limbal neoformation, microtia and skeletal deformities: a case report and literature review
- Goldenhar Syndrome: An Atypical Presentation With Developmental and Speech Delay
- Goldenhar Syndrome: Quality-of-Life Analysis of 43 Consecutive Patients
- Hemifacial Microsomia
- Hemifacial microsomia with extensive ipsilateral white matter hyperintensity
- Hemifacial microsomia: treatment alternatives-a systematic review of literature
- Identification of a de novo PUF60 variant associated with craniofacial microsomia
- Identification of novel mutations in EYA3 and EFTUD2 in a family with craniofacial microsomia: evidence of digenic inheritance
- Kaban-Pruzansky Grade Predicts Airway Severity in Hemifacial Microsomia
- Lacrimal Drainage Anomalies in Goldenhar, Rubinstein-Taybi, and Ectodermal-Ectrodactyly-Clefting Syndromes
- Loeys-Dietz syndrome and Goldenhar syndrome unveiled together
- Management of sleep-disordered breathing in patients with syndromic hemifacial macrosomia
- Management of unilateral craniofacial microsomia with orthopaedic functional appliances: A systematic literature review
- Model test study on treatment of Pruzansky type B and hemifacial microsomia with artificial condyle-mandibular distractor complex
- Model test study on treatment of Pruzansky type ⅡB and Ⅲ hemifacial microsomia with artificial condyle-mandibular distractor complex
- Modified horizontal muscle transposition without tenotomy and splitting for a case of inferior rectus and inferior oblique muscles aplasia with hemifacial microsomia
- Modified Nishida's procedure for esotropia in Duane syndrome associated with Goldenhar syndrome
- Morphologic Changes of the Temporomandibular Joint in Pruzansky-Kaban Type IIa Hemifacial Microsomia Postmandibular Distraction Osteogenesis
- Morphological and quantitative study of the inferior alveolar nerve canal in hemifacial microsomia
- Morphological integration in inferior alveolar canal and mandibular shapes
- Navigating Complexity in Mandibular Condyle Aplasia and Temporomandibular Joint Ankylosis in a Five-Year-Old Child: A Case Report
- Non-progressive mandibular changes in children with Type I and II craniofacial microsomia
- Oculo Auriculo Vertebral Spectrum
- Oculo auriculo vertebral spectrum and CHARGE association
- Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature review
- Orthodontic and Facial Characteristics of Craniofacial Syndromic Children with Obstructive Sleep Apnea
- Overlapping Spectrum of Craniofacial Microsomia Phenotype in Cat-Eye Syndrome
- Prenatal findings in 11 cases with craniofacial microsomia using the Alberta Congenital Anomalies Surveillance System, 1997-2019
- Quantitative Analysis on Cartilage Growth Between Ipsilateral and Contralateral Donor Sites in Microtia Patients
- Radiomics and Artificial Intelligence Study of Masseter Muscle Segmentation in Patients With Hemifacial Microsomia
- Respiratory outcome of mandibular distraction osteogenesis on obstructive sleep apnea in craniofacial microsomia: A retrospective study
- Rhabdomyomatous Mesenchymal Hamartoma: Report of 4 Cases With Histochemical and Immunohistochemical Findings and Emphasis on Potential Pitfalls
- Risk factors and characteristics of the birth of patients with craniofacial microsomia, a case-control study
- School participation among young people with craniofacial microsomia and other childhood-onset disabilities
- Sequential treatment of oral and maxillofacial deformities with hemifacial microsomia
- Single-stage Repair of Bilateral Cleft Lip and Bilateral Transverse Facial Cleft in Goldenhar Syndrome: A Case Report
- Soft-tissue, non-osteogenic distraction of the mandible and lower face in bilateral hemifacial microsomia-technical report
- Tessier Number 9 Craniofacial Cleft Associated with Goldenhar Syndrome and Its Surgical Management: A Report of a Rare Case
- The Chimeric LFC and DCIA Flap in Combined Mandibular and Condylar Head and Neck Reconstruction-A Case Series
- The etiology, clinical features, and treatment options of hemifacial microsomia
- Three-dimensional Analysis of the Temporal Bone Morphology in Patients with Craniofacial Microsomia
- Total temporomandibular joint reconstruction prosthesis in hemifacial microsomia: A systematic review
- Treatment of mild hemifacial microsomia in children by autologous nano-fat mixed granule fat transplantation
- Upper and Lower Limb Anomalies in Craniofacial Microsomia and Its Relation to the OMENS+ Classification: A Multicenter Study of 688 Patients
- Useful Genioplasty for Repeated Recurrent Sleep Apnea of Congenital Anomalies and Its Evaluation
- Using a New Deep Learning Method for 3D Cephalometry in Patients With Hemifacial Microsomia
- Vascular variation of temporoparietal fascia in microtia associated with hemifacial microsomia
- Velopharyngeal dysfunction and speech-related characteristics in craniofacial microsomia: a retrospective analysis of 223 patients
- Velopharyngeal insufficiency, speech, and language impairment in craniofacial microsomia: a scoping review