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3,978 Possible Causes for Kidney Disease, Thrombocytopenia

  • Paroxysmal Nocturnal Hemoglobinuria

    The combination of thrombosis, splenomegaly, and thrombocytopenia (TST) is challenging because anticoagulants are indicated but thrombocytopenia may increase the bleeding[] The association of Fanconi syndrome (FS) and chronic kidney disease (CKD) has been rarely described during the course of paroxysmal nocturnal hemoglobinuria (PNH).[] Fanconi syndrome and chronic kidney disease associated with paroxysmal nocturnal hemoglobinuria is rarely reported.[]

  • Congenital Hepatic Fibrosis

    We describe the first case of CHF presenting in an otherwise healthy child, with thrombocytopenia and splenomegaly as the only manifestations of the disease.[] […] autosomal-dominant polycystic kidney disease.[] In view of the persistent hypoprothrombinaemia, severe thrombocytopenia, and the multiple fistulas the risk of operation was thought to be unacceptable and she continues on[]

  • Congenital Acquired Immune Deficiency Syndrome

    Hepatitis Nephropathy Persistent fever lasting more than one month Neutropenia ( 1,000/µL), thrombocytopenia ( 100,000/µL) or anemia ( 8 g/dL).[] disease tumors or malignant lesions Q: What are our treatment options?[] ., inflammatory bowel disease, autoimmune thrombocytopenia, and autoimmune thyroid disease.[]

  • Uremia

    In addition, thrombocytopenia can also be induced by the heparin used during these procedures. Copyright 2017, 2013 Decision Support in Medicine, LLC.[] Disorders Associated with Chronic Kidney Disease Stage III-IV (Systematic Review and Meta-Analysis) By L.[] […] may include: Blood clotting problems Hemolytic anemia Kidney failure Hypertension leading to seizures, irritability, and other nervous system problems Too few platelets ( thrombocytopenia[]

  • Lupus Erythematosus

    […] autoimmune thrombocytopenia).[] Lupus patients do as well with these treatments as people who have other types of kidney disease. Many patients with lupus nephritis have received a kidney transplant.[] Hematologic evaluation typically reveals anemia, leukopenia, and thrombocytopenia. Urinalysis typically reveals proteinuria, hematuria, and casts.[]

  • Purpura

    The treatment of refractory immune-mediated thrombocytopenia purpura (ITP) can be challenging.[] kidney disease.[] Acquired thrombotic thrombocytopenia purpura is very rarely encountered in children. It is often misdiagnosed initially when the condition is not inherited.[]

  • Vitamin B12 Deficiency

    thrombocytopenia were improved by vitamin B12 supplementation alone, with a single session of plasma exchange.[] Some people shouldn’t take metformin, including people with kidney disease, liver disease, or congestive heart failure , for example, because of an increased risk of a potentially[] Some people shouldn’t take metformin, including people with kidney disease, liver disease, or congestive heart failure, for example, because of an increased risk of a potentially[]

  • Hyperkalemia

    Adverse effects of three different forms of heparin therapy: Thrombocytopenia, increased transaminases, and hyperkalaemia. Eur J Clin Pharmacol 1989 ;37: 415 – 8.[] Patiromer, a nonabsorbed potassium binder, decreases serum potassium in patients with chronic kidney disease on renin-angiotensin system inhibitors.[] PURPOSE OF REVIEW: Patients with chronic kidney disease (CKD) have an increased risk of hyperkalemia that increases both short-term and long-term mortality.[]

  • Malignant Hypertension

    Thrombotic thrombocytopenia purpura (TTP) is a rare clinical syndrome characterized by microangiopathic hemolytic anemia (MAHA), thrombocytopenia, neurologic symptoms, acute[] Chronic kidney disease leading to malignant hypertension and hyperviscosity was diagnosed as the underlying cause.[] Early performance of plasmapheresis can be justified in the presence of both TMA and thrombocytopenia.[]

  • Atypical Hemolytic Uremic Syndrome

    From Wikidata Jump to navigation Jump to search complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction atypical[] KEYWORDS: C3 glomerulopathy; anti-complement therapies; atypical hemolytic uremic syndrome; complement; glomerulonephritis; kidney disease [Indexed for MEDLINE] Free full[] A 28-day-old female presented with gross hematuria and hypertension. aHUS was suspected based on anemia with schistocytes, thrombocytopenia, low C3, and acute kidney injury[]

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