eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hemolytic anemia |
| Comorbidity | C0035078|renal failure |
| Sentences | 11 |
| PubMedID- 21151550 | Hemolytic uremic syndrome (hus) is a microangiopathic hemolytic anemia often complicated by acute renal failure in children. |
| PubMedID- 22572665 | Possible cases were identified from hospital records by international classification of diseases, ninth revision, clinical modification (icd-9-cm) codes: 283.1 (hemolytic uremic syndrome); 584.x, 283.x, and 287.x (acute renal failure with hemolytic anemia and thrombocytopenia); and 446.6 and 008.x, or 446.6 and 009.x (ttp with diarrhea caused by e. coli or an unknown pathogen) [9]. |
| PubMedID- 24325340 | Patients who had at admission renal failure, other causes of hemolytic anemia, hepatocellular carcinoma, sepsis, and/or active bleeding, were excluded. |
| PubMedID- 23162276 | We report here a case of 26-year-old male who presented with history of recurrent acute renal failure associated with microangiopathic hemolytic anemia and thrombocytopenia. |
| PubMedID- 20056203 | Result(s): both patients developed a very rare complication after surgery of severe thrombocytopenia with microangiopathic hemolytic anemia leading to acute renal failure. |
| PubMedID- 25859355 | However, oxaliplatin may rarely result in acute tubular necrosis (atn) [2], renal tubular acidosis [3, 4] and hemolytic anemia with subsequent renal failure [5]. |
| PubMedID- 25797912 | Scleroderma renal crisis (src) is a life-threatening complication of systemic sclerosis (ssc) that is characterised by new-onset malignant hypertension and progressive acute renal failure, often with associated microangiopathic haemolytic anaemia and thrombocytopenia. |
| PubMedID- 20948827 | It is characterised by microangiopathic haemolytic anaemia with thrombocytopenia and renal failure and is distinguished from classical diarrhoea-associated hus typically occurring in childhood (caused by shiga-toxin-producing bacteria and with a good prognosis; >90% children recover normal renal function with supportive therapy) and characterized by its chronic and relapsing course. |
| PubMedID- 21270465 | Like ddd, ahus is a rare inheritable chronic kidney disease caused by complement hyperactivity; but ahus is characterized by microvascular endothelial cell activation, thrombocytopenia, and hemolytic anemia leading to end-stage renal failure (29). |
| PubMedID- 24711939 | To our knowledge, this is the first such case of renal failure and jaundice without methemoglobinemia or hemolytic anemia in an adult patient with normal renal function. |
| PubMedID- 20981310 | However, the association of normotensive renal failure with microangiopathic hemolytic anemia in ssc was indicated [23]. |
Page: 1