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A case report of interventricular hemorrhage in William-Beuren syndrome
BACKGROUND: Williams syndrome (WS) (also as known Williams-Beuren Syndrome) is a neurodevelopmental disorder caused by deletion of chromosomes 7q11.23. WS phenotype is very variable but usually it is associated with a distinctive pattern of cognitive abilities. CASE PRESENTATION: 9-year-old female p...
Autores principales: | Alghobaishi, Abdullah, Mousa, Ahmed Hafez, Almonaye, Haleema Sami, Maghrebi, Tasneem Khalid, Amin, Abeer, Al Sharif, Fawziah Alzaid |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9422350/ https://www.ncbi.nlm.nih.gov/pubmed/36045762 http://dx.doi.org/10.1016/j.amsu.2022.104305 |
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