Weaver Syndrome: A Rare Cause of Neonatal Macrosomia and Dysmorphism. A Case Report.
Weaver syndrome is a rare genetic disorder characterized by abnormally excessive growth both in utero and postnatally. It is associated with a mutation in the EZH2 gene, which leads to accelerated bone development and other clinical manifestations such as macrocephaly, a characteristic dysmorphic...
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| Váldodahkkit: | , |
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| Materiálatiipa: | Artigo |
| Giella: | Árabe |
| Almmustuhtton: |
Algerian Society of Clinical & Oncological Pharmacy
2025-06-01
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| Ráidu: | Batna Journal of Medical Sciences |
| Fáttát: | |
| Liŋkkat: | https://batnajms.net/wp-content/uploads/Archives/2025/2/BJMS_Guellouh.pdf |
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