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A case of Beckwith-Wiedemann syndrome treated by tongue reduction
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- TAKANO Masayo
- Dental and Oral Medical Center, Kurume University School of Medicine
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- KOGA Makoto
- Dental and Oral Medical Center, Kurume University School of Medicine
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- TODOROKI Keita
- Dental and Oral Medical Center, Kurume University School of Medicine
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- AOKI Nobuko
- Dental and Oral Medical Center, Kurume University School of Medicine
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- NAKAMURA Mariko
- Dental and Oral Medical Center, Kurume University School of Medicine
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- KUSUKAWA Jingo
- Dental and Oral Medical Center, Kurume University School of Medicine
Bibliographic Information
- Other Title
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- 舌縮小術を行ったBeckwith-Wiedemann症候群の1例
- ゼツ シュクショウジュツ オ オコナッタ Beckwith-Wiedemann ショウコウグン ノ 1レイ
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Description
Beckwith-Wiedemann syndrome, also called EMG syndrome, is characterized by exomphalos, macroglossia, and gigantism. Here we report a case of Beckwith-Wiedemann syndrome accompanied with macroglossia in a 14-year-old male.<br>The patient was referred to our hospital for macroglossia and malocclusion in March 2008. The patient was diagnosed with Beckwith-Wiedemann syndrome by the clinical features: exomphalos, inguinal hernia, cryptorchism, macroglossia, and ear creases.<br>The patient underwent Egyedi-Obwegeser glossectomy under general anesthesia in February 2009, and was discharged from our hospital without any subjective complaints. At the time of this report, the patient had been followed up for 22 months. There has been no evidence of recurrence and the occlusion has been improving.
Journal
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- Journal of The Japanese Stomatological Society
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Journal of The Japanese Stomatological Society 61 (1), 54-58, 2012
Japanese Stomatological Society
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Details 詳細情報について
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- CRID
- 1390282681413414144
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- NII Article ID
- 130004555767
- 10030795738
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- NII Book ID
- AN00189050
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- ISSN
- 21850461
- 00290297
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- NDL BIB ID
- 023585049
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL Search
- CiNii Articles
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- Abstract License Flag
- Disallowed