[HTML][HTML] Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
D Solanki, P Fulzele, N Bhola - Cureus, 2023 - ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
D Solanki, P Fulzele, N Bhola - Cureus, 2023 - europepmc.org
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
[PDF][PDF] Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
D Solanki, P Fulzele, N Bhola, DR Solanki - Cureus, 2023 - cureus.com
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
[PDF][PDF] Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
D Solanki, P Fulzele, N Bhola - 2023 - assets.cureus.com
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
S Dhruvi, F Punit, B Nitin - Cureus, 2023 - search.proquest.com
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
D Solanki, P Fulzele, N Bhola - Cureus, 2023 - pubmed.ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
[PDF][PDF] Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report
D Solanki, P Fulzele, N Bhola - 2023 - assets.cureus.com
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
Management of Macroglossia Secondary to Beckwith-Weidmann Syndrome in a Pediatric Patient: A Case Report.
D Solanki, P Fulzele, N Bhola - Cureus, 2023 - europepmc.org
Beckwith-Wiedemann syndrome (BWS) is a rare genetic disorder, distinguished by the
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …
following characteristics: macrosomia, macroglossia, abdominal wall deformities such as …