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Diagnosis and Management of Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann syndrome (BWS) is a human genomic imprinting disorder that presents with a wide spectrum of clinical features including overgrowth, abdominal wall defects, macroglossia, neonatal hypoglycemia, and predisposition to embryonal tumors. It is associated with genetic and epigenetic cha...
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| Publicat a: | Front Pediatr |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6990127/ https://ncbi.nlm.nih.gov/pubmed/32039119 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2019.00562 |
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