Introduction: While severe macroglossia in Beckwith-Wiedemann syndrome (BWS) is often treated with tongue reduction surgery, most patients with mild to moderate macroglossia are nonsurgically managed. Given that outcomes for these conservatively managed patients are not well characterized, this study aims to describe the natural history of patients with macroglossia and BWS who did not undergo early surgery.
Methods: Records of patients with BWS and macroglossia seen between 2004-2024 were reviewed. Conservative management was defined as not having had surgery during the first 3 years of life. Macroglossia was rated using the BWS Index of macroGlossia (BIG) scale to stratify phenotypic severity. Relationships among polysomnography data, surgical incidence, percentage mosaicism, and clinical scores were assessed.
Results: 320 patients with BWS and macroglossia were included, 231 (72.2%) of whom were conservatively managed. As BIG scores increased from BIG1 (mild) to BIG2 (moderate) to BIG3 (severe), both obstructive sleep apnea severity (P < .001) and surgical incidence increased (P < .001). Among conservatively managed patients, obstructive apnea-hypoxia index improved from 4.5 (interquartile range: 2.7-11.2) events per hour (age 0.4 [0.2-0.7] years) to 3.6 (1.3-6.1) events per hour (age 2.2 [1.7-2.6] years; P = .03). BIG scores also improved in this cohort from 2.0 (1.0-2.0) at 0.8 (0.4-1.5) years of age to 1.0 (1.0-2.0) at 2.6 (2.2-3.7) years of age (P = .02).
Conclusion: Nonsurgical management in the first 3 years of life for mild and moderate macroglossia in BWS is associated with favorable outcomes. Obstructive sleep apnea and macroglossia often improve as the facial skeleton grows to accommodate the tongue.
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http://dx.doi.org/10.1542/peds.2024-068618 | DOI Listing |
Pediatrics
March 2025
Division of Plastic, Reconstructive, and Oral Surgery, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Introduction: While severe macroglossia in Beckwith-Wiedemann syndrome (BWS) is often treated with tongue reduction surgery, most patients with mild to moderate macroglossia are nonsurgically managed. Given that outcomes for these conservatively managed patients are not well characterized, this study aims to describe the natural history of patients with macroglossia and BWS who did not undergo early surgery.
Methods: Records of patients with BWS and macroglossia seen between 2004-2024 were reviewed.
JCEM Case Rep
January 2025
Department of Endocrinology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
A male neonate exhibited hallmark features of Beckwith-Wiedemann syndrome (BWS) including large for gestational age, macroglossia, multiple ear pits, and umbilical hernia. He had neonatal hypoglycemia, requiring a glucose infusion rate of 9.7 mg/kg/min.
View Article and Find Full Text PDFJ Craniofac Surg
January 2025
Division of Plastic Surgery, Department of Surgery, Dalhousie University.
Introduction: Macroglossia is a frequent clinical feature of Beckwith-Wiedemann syndrome (BWS), a congenital overgrowth disorder. Macroglossia can lead to abnormal breathing, feeding, speech, and dentoskeletal development. Partial glossectomy is a common intervention aimed at reducing these abnormalities.
View Article and Find Full Text PDFOrphanet J Rare Dis
October 2024
Division of Human Genetics, Children's Hospital of Philadelphia, 3401 Civic Center Blvd, Philadelphia, PA, 19104, USA.
Background: An easy-to-use tool to objectively measure intraoral anatomy with meaningful clinical correlations may improve care for patients with Beckwith-Wiedemann syndrome (BWS), who commonly have symptomatic macroglossia.
Methods: Children aged 2-17 years with BWS were enrolled between 12/2021 and 01/2024. Digital intraoral photographs with a laser ruler were taken, and morphometric measurements were made using ImageJ software.
Int J Clin Pediatr Dent
June 2024
Department of Oral Medicine and Radiology, Mahatma Gandhi Dental College and Hospital, Jaipur, Rajasthan, India.
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