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29 Possible Causes for Immunoglobulin G Decreased, Lupus Nephritis

Did you mean: immunoglobulin a decreased, lupus nephritis

  • Nephrotic Syndrome

    These can include: membranous nephropathy, focal segmental glomerulosclerosis, minimal change disease, membranoproliferative glomerulonephritis, lupus nephritis, and IgA nephropathy[] It generally affects more men than women although lupus nephritis is common in women. It affects more adult than children with an estimated adult:child ratio of 26:1.[] ., IgA nephropathy), fibrillary glomerulopathies (the most common being amyloidosis), lupus nephritis, and multiple myeloma (e.g., light-chain deposition diseases). [16] Hull[]

  • Methylprednisolone

    Severe lupus nephritis . Adults: 1 g I.V. over 1 hour for 3 days. Therapy is then continued orally at 0.5 mg/kg daily.[]

  • Ataxia Telangiectasia

    Nephritis Pias1 Arsenic Poisoning , Brain Injuries , focal segmental glomerulosclerosis , Skin Diseases Ppm1d Brain Stem Neoplasms , Breast Neoplasms , glioma , INTELLECTUAL[] Nephritis Otub1 Lymphoma Atm Lymphoma, B-Cell Atm , Kat5 Lymphoma, Mantle-Cell Atm Lymphoma, T-Cell, Cutaneous Atm Lymphoma, T-Cell, Peripheral Atm Mammary Neoplasms, Animal[] Ppp2ca Liver Reperfusion Injury H2afx Long QT Syndrome Ubr5 lung adenocarcinoma Mre11a Lung agenesis Eya1 Lung Neoplasms Kdm4a , Mdc1 lung squamous cell carcinoma Ppp6c Lupus[]

  • Lupus Nephritis

    Class II: Mesangial proliferative lupus nephritis Class III: Focal proliferative lupus nephritis  Class IV: Diffuse proliferative lupus nephritis  Class V: Membranous lupus[] All patients with Lupus nephritis have proteinuria.[] […] and sclerosing lupus nephritis Class III (C) : Chronic inactive lesions with glomerular scars: Focal sclerosing lupus nephritis Class IV : Diffuse lupus nephritis Active[]

  • Immunosuppressive Drug

    lupus nephritis,” lead author Candace Feldman, MD, MPH, assistant professor of medicine, Harvard Medical School in Boston, and associate physician at Brigham and Women’s[] Abatacept Orencia second-generation belatacept Prescribed for Renal transplant RA, UC, lupus nephritis 57. CP-690,550 JAK3 inhibitor 58. Phase II treatment RA 59.[] It is now also prescribed for people who suffer from inflammation of the kidney caused by lupus, otherwise known as lupus nephritis.[]

  • Protein Losing Enteropathy

    Twenty-five PLE patients (56.8%) had concomitant lupus nephritis (LN). Of these, seven patients underwent renal biopsy.[] Wu CC, Lin SH, Chu P, Lai JH, Chang DM, et al. (2004) An unrecognized cause of oedema in a patient with lupus nephritis: protein losing enteropathy.[] Most PLE-related GI manifestations are not as common as other organ involvement such as lupus nephritis, and PLE is clinically indistinguishable from nephrotic syndrome [3[]

  • Renal Amyloidosis

    The patient was admitted to the Internal Medicine Department to evaluate the etiology of the nephrotic syndrome, among which the possibilities were: lupus nephritis, amyloidosis[]

  • Immune Thrombocytopenic Purpura

    Clinical-Pathological Features and Prognosis of Thrombotic Thrombocytopenic Purpura in Patients With Lupus Nephritis. Am J Med Sci . 2009 Sep 9. [Medline] .[] It is mediated by immune mechanisms, in most cases immunoglobulin g autoantibodies which attach to platelets and subsequently undergo destruction by macrophages.[] Bleeding or bruising tendency due to low platelet level Thrombocytopenia occurring in the absence of toxic exposure or a disease associated with decreased platelets.[]

  • Adrenal Cortex Hormone

    Lupus Nephritis Corticosteroid therapy is a major component in therapeutic regimens for systemic lupus erythematosus (SLE).[] Patients with chronic incurable diseases such as systemic lupus erythematosus or nephritis need a clear plan of when, how much and for how long corticosteroid therapy is required[] Although most clinical trials of corticosteroid therapy in SLE patients have been conducted in patients with severe lupus nephritis, the evidence suggests that they are also[]

  • Systemic Amyloidosis

    nephritis, and thrombotic microangiopathy.[] 52 Fibrils can also be found in hereditary nephropathies with fibronectin, and collagenofibrotic glomerulopathy, diabetic nephropathy (so called “diabetic fibrillosis”), lupus[]

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