PedAM
Pediatric Disease Annotations & Medicines
| Disease | liver disease |
| Phenotype | C0037061|siderosis |
| Sentences | 4 |
| PubMedID- 20739079 | Beta-globin mutations are associated with parenchymal siderosis and fibrosis in patients with non-alcoholic fatty liver disease. |
| PubMedID- 26331014 | Neonatal hemochromatosis (nh) is defined by liver disease associated with siderosis of the extrahepatic tissues 1. the most frequent cause of nh is a gestational alloimmune disorder called gestational alloimmune liver disease, which results from the transplacental transfer of maternal immunoglobulin g (igg) antibodies 2. although about 80% of nh patients can survive without liver transplantation because of exchange transfusions and intravenous ig therapy, some of the patients with more serious disease require transplantation 3. occasionally, severely affected nh infants exhibit renal tubular dysgenesis (rtd) 4. nh with rtd has been reported in only five cases, all of which were stillborn or resulted in early neonatal death 5–8. |
| PubMedID- 22322235 | Neonatal iron overload and tissue siderosis due to gestational alloimmune liver disease. |
| PubMedID- 20801540 | 4b mean hepcidin mrna levels and hepcidin/log (ferritin) ratios are higher in acp, dysmetabolic siderosis, and patients with fatty liver disease as compared to patients with c282y homozygous hemochromatosis or viral hepatitis. |
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