Beckwith-Wiedemann Syndrome in a Premature Dizygotic Female Twin: A Case Report
Beckwith-Wiedemann Syndrome is a congenital disease that is rare and has low prevalence worldwide. It presents classically with features of macroglossia, abdominal wall defects (omphalocele), and macrosomia at birth. Other typical manifestations include facial nevus simplex, ear lobe abnormalities (...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Surgical Society of Kenya
2022-01-01
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| Series: | The Annals of African Surgery |
| Subjects: | |
| Online Access: | https://www.annalsofafricansurgery.com/copy-of-beckwith-wiedemann-syndrome |