• (Epi)genotype and Timing of Tongue Reduction Predict Safety and Long-Term Outcomes in Beckwith-Wiedemann Syndrome
• "Snail-Track Ulcers" And Macroglossia Due to Secondary Syphilis
• A Case Report of a Filipino Boy with Childhood Cataract and Clinically Diagnosed Roberts Syndrome
• A Delayed Diagnosis of Myxedema Coma
• A Novel Macroglossia Severity Index for Beckwith-Wiedemann Syndrome
• A rare case of extremely low birth weight infant with Beckwith-Wiedemann syndrome
• Adult experiences in Beckwith-Wiedemann syndrome
• Amyloid Deposition in the Upper Aerodigestive Tract, A Single Institute Experience
• Amyloidosis
• Amyloidosis
• Amyloidosis initially only manifesting as oral mucosal hemorrhagic lesions: a case series report
• An idiopathic severe macroglossia in a young adult patient: a rare case
• Application of bilateral condylectomy as an alternative surgical treatment for Class III malocclusion with posterior vertical excess, a technical note
• Application of Original Therapy for Stimulation of Oral Areas Innervated by the Trigeminal Nerve in a Child with Beckwith-Wiedemann Syndrome
• Assessment of Preoperative Predictors for Difficult Laryngeal Exposure in Endolaryngeal Surgery
• Associations between the timing of tongue reduction surgery, (Epi)genotype, and dentoskeletal development in patients with Beckwith-Wiedemann syndrome
• Avalglucosidase alfa in infantile-onset Pompe disease: A snapshot of real-world experience in Italy
• Beckwith-Widemann Macroglossia: The Role of Surgical Tongue Reduction
• Beckwith-Wiedemann Syndrome
• Beckwith-Wiedemann syndrome
• Beckwith-Wiedemann Syndrome
• Beckwith-Wiedemann syndrome in a child with multifocal Wilms tumor and lateralized overgrowth: A case report
• Beckwith-Wiedemann Syndrome in Newborn of Mother with HELLP Syndrome/Preeclampsia: An Analysis of Literature and Case Report with Fetal Growth Restriction and Absence of <em>CDKN1C</em> Typical Pathogenic Genetic Variation
• Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening
• Beckwith-Wiedemann syndrome with multiple hepatic and cutaneous hemangiomas in a female patient of Albanian origin: Diagnostic and therapeutic considerations
• Beckwith-Wiedemann Syndrome With Severe Relapsing Hypoglycemia After the Neonatal Period: A Case Report and a Literature Review
• Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry
• Case 16: A 75-Year-Old Man With Macroglossia and Hypercalcemia
• CASK pathogenic variant which expands the clinical spectrum for MICPCH syndrome in an adult patient
• Cerebrocostomandibular syndrome: a diagnostic challenge
• Clinical relevance of macroglossia to disease progression in ventilation dependent patients with advanced ALS
• Clinical, Phenotypic, and Demographic Characteristics of Peruvian Children and Neonates with Autosomal and Sex Chromosome Aneuploidies
• Coexistence of variant-type transthyretin and immunoglobulin light-chain amyloidosis: a case report
• Comprehensive Preventive and Therapeutic Oral Health Care: A Case Report of Mucopolysaccharidosis Type IV A in a Pediatric Patient
• Comprehensive review of the timing of surgical management of macroglossia in Beckwith-Wiedemann syndrome
• Concurrent Papillary Craniopharyngioma and Growth Hormone-Secreting Pituitary Adenoma: A Rare and Aggressive Collision Tumor
• CT volumetric analysis permits comparison of tongue size and tongue fat in different canine brachycephalic and mesaticephalic breeds
• Dentoskeletal features and growth pattern in Beckwith-Wiedemann spectrum: is surgical tongue reduction always necessary?
• Dystrophin (<em>DMD</em>) Missense Variant in Cats with Becker-Type Muscular Dystrophy
• Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome
• Enzyme replacement therapy and immunotherapy lead to significant functional improvement in two children with Pompe disease: a case report
• Evaluation of keyhole-pattern reduction glossoplasty for macroglossia in beckwith-wiedemann syndrome: A multidimensional analysis of postoperative course and outcomes
• Expanded phenotype and cancer risk in patients with Beckwith-Wiedemann spectrum caused by CDKN1C variants
• Failed Tracheal Extubation Due to Transient Isolated Macroglossia in a Child
• Features of Obstructive Sleep Apnea in Children with and without Comorbidities
• Feline dystrophin-deficient muscular dystrophy misdiagnosed as <em>Toxoplasma</em> myositis
• Fragile lip in a patient with macroglossia due to hemodialysis-associated amyloidosis
• Giant tongue leading to dysphagia in light chain amyloidosis patient
• Glossectomy
• Glossectomy
• Hereditary transthyretin amyloidosis presenting with spontaneous periorbital purpura: a case report
• Histotoxicity induced by copper oxide nanoparticles (CuO-NPs) on developing mice (Mus musculus)
• Hypothyroidism presenting as a fissure tongue
• Individualized treatment of congenital vascular malformations of the tongue
• Infant with macroglossia
• Infantile hypothyroidism and its relationship with delayed tooth eruption: A case report
• Interdisciplinary Treatment of Macroglossia Due to a Microcystic Lymphatic Malformation with Bleomycin Electrosclerotherapy Followed by Partial Resection
• Introduction to the Beckwith-Wiedemann Syndrome and Cancer Special Issue
• Investigation of a pervasive immune, cardiac, and behavioral phenotype in Beckwith-Wiedemann syndrome: A case report
• Kleefstra Syndrome-Dental Manifestations and Needs: A Case Report with a Literature Review
• Lingual Abscess after Posterior Fossa Surgery: An Unusual Complication of the Concorde Position
• Long-Term Follow-up With Multispecialty Management of a Giant Lymphangioma of an Infant Tongue Contributed to Reduced Complications of the Disease: A Case Report of a 21-Year Follow-up
• Macroglossia
• Macroglossia
• Macroglossia and lip edema: A case of paraproteinemia-associated scleredema responsive to intravenous immunoglobulins
• Macroglossia in endocrine and metabolic disorders: current evidence, perspectives and challenges
• Macroglossia: compressiontherapy as an alternative treatment option
• Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
• Methodical control of the difficult pediatric airway: two case reports
• Microperimetric evaluation for different methods of epiretinal membrane surgery
• Multiple myeloma initially manifesting as a solitary deep ulcer on the tongue: a case study and literature review
• Multisystem approach for management of OSA in Down syndrome: a case report
• Nasopharyngeal Airway
• Nasopharyngeal Airway
• Nasotracheal intubation awake in a patient with multiple fractures of the maxilla and cervical spine: A case report
• Open Bite Malocclusion and Orofacial Dysfunction in Patients with Myotonic Dystrophy Type 1 and Duchenne Muscular Dystrophy
• Oral amyloidosis: an update
• Oral Structural Dysphagia in Children
• Orofacial myofunctional therapy associated with the use of the stimulating palatal plate in children with trisomy 21: case studies
• Orofacial symptoms suggestive of malignant lesions and the role of imaging: literature review and case presentation
• Partial amputation due to tongue bite in death-associated with eclampsia
• Pediatric cancer incidence among individuals with overgrowth syndromes and overgrowth features: A population-based assessment in seven million children
• Phenotype Genotype Characterization of FKRP-related Muscular Dystrophy among Indian Patients
• Phenotypic spectrum and tumor risk in Simpson-Golabi-Behmel syndrome: Case series and comprehensive literature review
• Polyhydramnios associated with rare genetic syndromes: two case reports
• Precision medicine using whole genome sequencing identifies a novel dystrophin (DMD) variant for X-linked muscular dystrophy in a cat
• Preterm with Macroglossia and Persistent Hypoglycemia - Beckwith-Wiedemann Syndrome
• Radiographic, MRI, and CT findings in a young dog with Becker-like muscular dystrophy
• Rare but Real: Severe Unilateral Macroglossia and Submandibular Sialoadenitis After Skull Base Surgery
• Recurrent <em>PIK3CA H1047R</em>-Mutated Congenital Infiltrative Facial Lipomatosis: A Case Report and Review of Literature
• Sturge-Weber syndrome with massive macroglossia and anterior neck space infection- a case report and review of literature
• Supernumerary chromosome 6 marker associated with paternal uniparental isodisomy of chromosome 6 in a patient with a syndromic disorder of insulin secretion
• The Efficacy of the Partial Glossectomy for Prevention of Airway Volume Reduction in Orthognathic Surgery of Class III Patients
• The Influence of the Tongue on the Development of Dental Malocclusion
• The role of pediatric oncologist in prenatal diagnosis: A 10-year retrospective study at Assistance Publique Hôpitaux de Marseille (AP-HM)
• Tongue and Mandibular Disorders of the Pediatric Patient
• Trends in Blood Mosaicism and Clinical Phenotype Score in Patients with Beckwith-Wiedemann Syndrome Evaluated for Tongue Reduction Surgery
• Two emerging phenotypes of atypical inclusion body myositis: illustrative cases
• Unusual Presentation of Beckwith-Wiedemann Syndrome in an Extremely Low Birth Weight Infant
• What to Expect of Feeding Abilities and Nutritional Aspects in Achondroplasia Patients: A Narrative Review