hemolytic anemia diagnosis

May 19, 2016

Wegener’s granulomatosis and microscopic polyangiitis

Posted by: adminIn: Infectious DiseasesTags: & III autoimmune polyglandular syndromes, chronic, goodpasture syndrome prognosis, goodpasture syndrome survival rate, goodpasture syndrome treatment, goodpasture’s syndrome, granulomatosis with polyangiitis, granulomatosis with polyangiitis and microscopic polyangiitis, granulomatosis with polyangiitis causes, granulomatosis with polyangiitis icd 10, granulomatosis with polyangiitis patient uk, granulomatosis with polyangiitis review, Graves Disease, Graves Disease Treatment, graves’ disease (hyperthyroidism), graves’ disease is a result of, graves’ disease is caused by, graves’ disease overactive thyroid gland, guillain-barré syndrome, guillain-barré syndrome and zika virus, guillain-barré syndrome zika, hashimoto encephalopathy mri, Hashimoto's Thyroiditis, hashimoto's encephalitis mayo clinic, hashimoto's encephalopathy emedicine, hashimoto's encephalopathy symptoms, hashimoto’s encephalitis, hashimoto’s thyroiditis and atrophic thyroiditis, hashimoto’s thyroiditis and hives, hashimoto’s thyroiditis diagnosis, hashimoto’s thyroiditis icd 10, hemolytic anemia, hemolytic anemia classification, hemolytic anemia definition, hemolytic anemia diagnosis, hemolytic anemia icd 10, hemolytic anemia in dogs, hemolytic anemia ppt, hemolytic anemia treatment, hemolytic anemia types, henoch-schonlein purpura, henoch-schonlein purpura (hsp), henoch-schönlein purpura in adults, henoch-schonlein purpura nephritis, henoch-schonlein purpura treatment, herpes gestationis, herpes gestationis definition, herpes gestationis during pregnancy, herpes gestationis pathology outlines, herpes gestationis pictures, herpes gestationis vs puppp, hypogammaglobulinemia, hypogammaglobulinemia causes, hypogammaglobulinemia icd 10, hypogammaglobulinemia icd 9, Idiopathic pulmonary fibrosis, idiopathic thrombocytopenic purpura (itp), idiopathic thrombocytopenic purpura (itp) causes the following manifestations except, idiopathic thrombocytopenic purpura (itp) is caused by, idiopathic thrombocytopenic purpura (itp) symptoms, iga nephropathy, iga nephropathy diagnosis, iga nephropathy icd 10, iga nephropathy medscape, iga nephropathy nhs, iga nephropathy treatment, iga nephropathy uptodate, igg4 related sclerosing disease treatment, igg4-related sclerosing disease, igg4-related sclerosing disease symptoms, II, Immunoregulatory lipoproteins, Inclusion body myositis, Interstitial cystitis, Juvenile arthritis, Juvenile diabetes (Type 1 diabetes), Juvenile myositis, Kawasaki syndrome, Lambert-Eaton syndrome, Leukocytoclastic vasculitis, Lichen planus, Lichen sclerosus, Ligneous conjunctivitis, Linear IgA disease (LAD), Lupus (SLE), Lyme disease, Meniere’s disease, Microscopic polyangiitis, Mixed connective tissue disease (MCTD), Mooren’s ulcer, Mucha-Habermann disease, multiple sclerosis, Myasthenia gravis, Myositis, narcolepsy, Neuromyelitis optica (Devic’s), Neutropenia, Ocular cicatricial pemphigoid, Optic neuritis, Palindromic rheumatism, PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcus), Paraneoplastic cerebellar degeneration, Paroxysmal nocturnal hemoglobinuria (PNH), Parry Romberg syndrome, Pars planitis (peripheral uveitis), Parsonnage-Turner syndrome, Pemphigus, peripheral neuropathy, Perivenous encephalomyelitis, Pernicious anemia, POEMS syndrome, Polyarteritis nodosa, Polymyalgia rheumatica, Polymyositis, Postmyocardial infarction syndrome, Postpericardiotomy syndrome, Primary biliary cirrhosis, Primary sclerosing cholangitis, Progesterone dermatitis, Psoriasis, Psoriatic arthritis, Pure red cell aplasia, Pyoderma gangrenosum, Raynauds phenomenon, Reactive Arthritis, Reflex sympathetic dystrophy, Reiter’s syndrome, Relapsing polychondritis, Restless legs syndrome, Retroperitoneal fibrosis, rheumatic fever, Rheumatoid Arthritis, Sarcoidosis, Schmidt syndrome, Scleritis, scleroderma, Sjogren’s syndrome, Sperm & testicular autoimmunity, Stiff person syndrome, Subacute bacterial endocarditis (SBE), Susac’s syndrome, Sympathetic ophthalmia, Takayasu’s arteritis, Temporal arteritis/Giant cell arteritis, Thrombocytopenic purpura (TTP), Tolosa-Hunt syndrome, Transverse myelitis, Type 1 diabetes, Type I, Ulcerative colitis, Undifferentiated connective tissue disease (UCTD), Uveitis, Vasculitis, Vesiculobullous dermatosis, Vitiligo, Wegener’s granulomatosis (now termed Granulomatosis with Polyangiitis (GPA)3

Wegener’s granulomatosis (also known as granulomatosis with polyangiitis) is a type of vasculitis that affects small and medium blood vessels. Symptoms can include saddle nose deformity, chronic sinusitis, and collapsed trachea. Microscopic polyangiitis is similar to wegener’s granulomatosis except it only affects small blood vessels in the lungs or kidneys. Learn how the presence of granulomas and antibodies (cANCA and pANCA) differentiate these two conditions.
More free lessons at: http://www.khanacademy.org/video?v=Ax98k35h_jk

Practice questions related to these concepts here:
https://www.khanacademy.org/test-prep/NCLEX-RN/rn-cardiovascular-diseases/rn-vasculitis/e/vasculitis-quiz

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These videos do not provide medical advice and are for informational purposes only. The videos are not intended to be a substitute for professional medical advice, diagnosis or treatment. Always seek the advice of a qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read or seen in any Khan Academy video.

May 19, 2016

Goodpasture syndrome (Medical Condition)

Symptoms, risk factors and treatments of Goodpasture syndrome (Medical Condition)

Goodpasture syndrome is a rare autoimmune disease in which antibodies attack the lungs and kidneys, leading to bleeding from the lungs and to kidney failure

This video contains general medical information If in doubt, always seek professional medical advice.
The medical information is not advice and should not be treated as such. The medical information is provided without any representations or warranties, express or implied. We do not warrant or represent that the medical information on this websiteis true, accurate, complete, current or non-misleading

Music: ‘Undaunted’ Kevin Macleod CC-BY-3.0
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May 19, 2016

MyUSMLE CK: Goodpasture syndrome

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May 19, 2016

Goodpasture syndrome

Goodpasture syndrome (GPS; also known as Goodpasture’s disease, anti-glomerular basement antibody disease, or anti-GBM disease) is a rare autoimmune disease in which antibodies attack the lungs and kidneys, leading to bleeding from the lungs and to kidney failure. It may quickly result in permanent lung and kidney damage, often leading to death. It is treated with immunosuppressant drugs such as corticosteroids and cyclophosphamide, and with plasmapheresis, in which the antibodies are removed from the blood.
The disease was first described by the American pathologist Ernest Goodpasture of Vanderbilt University, in 1919 and was later named in his honour.

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May 19, 2016

Goodpasture Syndrome

Goodpasture Syndrome
Instructional Tutorial Video
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URL: http://youtu.be/S2Iotn0Hye0

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