A Newly Identified Mutation in the WT1 Gene in Denys-Drash Syndrome
Denys-Drash syndrome (DDS) is a rare autosomal dominant disorder characterized by genital abnormalities, nephropathy, and Wilms’ tumor (WT), typically caused by heterozygous mutations in the Wilms’ tumor suppressor 1 (WT1) gene. Here, a 2-year-old male admitted with fever and abdominal pain was pres...
I tiakina i:
| Ngā kaituhi matua: | , , , , , |
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| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Duzce University
2025-12-01
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| Rangatū: | Düzce Tıp Fakültesi Dergisi |
| Ngā marau: | |
| Urunga tuihono: | https://dergipark.org.tr/en/download/article-file/4896051 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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