Alexandra Stanciu
Biographic Data
| ID | 10416289 |
|---|---|
| NAME | Alexandra Stanciu |
| GIVEN NAMES | Alexandra |
| FAMILY NAME | Stanciu |
| SIGNATURE | STANCIU A |
| AFFILIATIONS | Department of Pediatric Nephrology, “M.S. Curie” Emergency Clinical Hospital for Children, 077120 Bucharest, Romania |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 1 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2025 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 0 |
WT1-Related Nephropathy in a Phenotypically Female Child
WT1-related disorders comprise a spectrum of conditions resulting from mutations or deletions of the WT1 gene. Alteration in this gene have been associated with many syndromes, including WAGR syndrome, Denys-Drash syndrome (DDS), Frasier syndrome (FS) and Meacham syndrome. We present the case of an 8-year-old phenotypically female child with symptoms of end-stage kidney disease (ESKD), hypertension and anasarca, requiring renal replacement therap…
No prominent works on this page.
WT1-Related Nephropathy in a Phenotypically Female Child
WT1-related disorders comprise a spectrum of conditions resulting from mutations or deletions of the WT1 gene. Alteration in this gene have been associated with many syndromes, including WAGR syndrome, Denys-Drash syndrome (DDS), Frasier syndrome (FS) and Meacham syndrome. We present the case of an 8-year-old phenotypically female child with symptoms of end-stage kidney disease (ESKD), hypertension and anasarca, requiring renal replacement therap…
Bioinformatics (1 work) · Biology (1 work) · Disease (1 work) · Focal segmental glomerulosclerosis (1 work) · Gene (1 work) · Genetic and Kidney Cyst Diseases (1 work) · Genetics (1 work) · Glomerulonephritis (1 work) · Internal Medicine (1 work) · Kidney (1 work)