Yung-Han Hsu
Biographic Data
| ID | 10487062 |
|---|---|
| NAME | Yung-Han Hsu |
| GIVEN NAMES | Yung-Han |
| FAMILY NAME | Hsu |
| SIGNATURE | HSU Y |
| AFFILIATIONS | Department of Pediatrics, Hsinchu Municipal MacKay Children’s Hospital, Hsinchu City 300046, Taiwan |
| 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 |
Neonatal Pyruvate Kinase Deficiency Presenting with Severe Hemolytic Anemia and Liver Failure
Background : Pyruvate kinase deficiency (PKD) is the most prevalent enzymatic defect of the glycolytic pathway, causing chronic congenital non-spherocytic hemolytic anemia. Clinical severity ranges from mild anemia to transfusion-dependent diseases. Severe neonatal presentations, including liver failure, have rarely been reported. Case presentation: We report a preterm female neonate with PKD who developed early-onset hemolytic anemia, conjugated…
No prominent works on this page.
Neonatal Pyruvate Kinase Deficiency Presenting with Severe Hemolytic Anemia and Liver Failure
Background : Pyruvate kinase deficiency (PKD) is the most prevalent enzymatic defect of the glycolytic pathway, causing chronic congenital non-spherocytic hemolytic anemia. Clinical severity ranges from mild anemia to transfusion-dependent diseases. Severe neonatal presentations, including liver failure, have rarely been reported. Case presentation: We report a preterm female neonate with PKD who developed early-onset hemolytic anemia, conjugated…
Anemia (1 work) · Cancer, Hypoxia, and Metabolism (1 work) · Erythrocyte Function and Pathophysiology (1 work) · Exchange transfusion (1 work) · Hemoglobin structure and function (1 work) · Hemolysis (1 work) · Hemolytic anemia (1 work) · Liver failure (1 work) · Phenotype (1 work) · Pyruvate kinase (1 work)