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...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Árabe |
| Julkaistu: |
Algerian Society of Clinical & Oncological Pharmacy
2025-06-01
|
| Sarja: | Batna Journal of Medical Sciences |
| Aiheet: | |
| Linkit: | https://batnajms.net/wp-content/uploads/Archives/2025/2/BJMS_Guellouh.pdf |
| Tagit: |
Ei tageja, Lisää ensimmäinen tagi!
|