Abstract | BACKGROUND: CASE PRESENTATION: CONCLUSION: This unique case highlights HUS as a rare but important manifestation of WT1 mutation and provides new insight into the genetics underlying this association.
|
Authors | Joseph L Alge, Scott E Wenderfer, John Hicks, Mir Reza Bekheirnia, Deborah A Schady, Jamey S Kain, Michael C Braun |
Journal | BMC nephrology
(BMC Nephrol)
Vol. 18
Issue 1
Pg. 243
(Jul 18 2017)
ISSN: 1471-2369 [Electronic] England |
PMID | 28720077
(Publication Type: Case Reports, Journal Article)
|
Chemical References |
- WT1 Proteins
- WT1 protein, human
|
Topics |
- Denys-Drash Syndrome
(diagnosis, genetics, surgery)
- Diagnosis, Differential
- Female
- Hemolytic-Uremic Syndrome
(diagnosis, genetics, surgery)
- Humans
- Infant
- Mutation
(genetics)
- WT1 Proteins
(genetics)
|