Rwcmediaku.com - Cerito kalo ni aku buat atas pengamatan beberapa hari ini tentang tugas pak M.Hidayat,S.Kep,.M.Biomed Beliau meminta membuat tugas Tentang Respon Imun, beliau meminta membuat tugas dengan penyakit yg Judul-Nya kita tentukan sendiri,
2 Hari lalu, saya mengamati semakin banyak orang yg saling Klaim judul masing-masing ada Yg meng-Klaim ingin memakai, judul Hiv, Aids,Lupus(SLE), Malaria, dll..
Bahkan yg aneh bahkan unik sekali nih orang, sampai-sampai kebingungan mereka mengangkat judul, Kudis, Kurap, Panu,kadas, Emang itu respon imun ya,,,?
bahkan ada beberapa orang yg belum mendapat judul, Termasuk aku, belum dapat judul juga...
Mereka terlihat saling meng-Klaim judul masing-masing di Aplikasi Perpesanan Instan Milik BlackBerry.
Bahkan akibat saling meng-klaim judul, ada yg emosian, waduh....waduh...
Haduh, kalau saja mereka modern atau Update teknologi, bukan Update status yg tiap menit, bahkan tiap detik, maksud saya disini Update tentang Teknologi yg ada, Ingat Loh kita ini hidup di zaman modern, zaman yg serba Digital,Elektronik, Instan.. Yg apa-apa bisa dilakukan dari jauh, sebut saja, Mau mesan makanan tinggal Delivery.. mau transfer uang tinggal pakai M-Banking, Mau Pulsa Tingal pke M-Kios, Mau tanya Tugas M-Arasit,M-Noval (*hehhe yg ini bercanda kok ),
Saya yakin mereka itu selalu Update, Tapi Updatenya mungkin bukan ke hal yg saya maksud, Mungkin Loh ini Mungkin ingin Loh, kata lagu stinky, Mungkinkah....?
Mereka bisa saja bertanya ke Forum, baik itu Forum FB, Twitter, Khusus Website Forum Kesehatan, WaW... Kalau saya mau cerita, akan panjang nantinya, Mereka bisa juga menggunakan Seacrhing Engine yg biasa mereka gunakan, Sebut saja Google, di Google Itu ada Google Tanya Jawab, Di Yahoo Seach Engine Ada Yahoo Tanya Jawab, Itu mereka bisa bertanya kalau mereka mau, orang-orang disana, saya akui Sangat ramah, Ini saya nilai selama saya bergaung di Yahoo Tanya Jwab Sejak Tahun 2010, saya merasa terbantu akan hadirnya fitur itu, bukan saya promosi ataupun membanggakan loh,
Mereka mikir judul tugas Respon Imun, udah kayak mikir Judul Skripsi aja. ckckkck....
Apakah mungkin tugas respon imun itu, judul yg harus kita pakai, adalah judul / Materi yg sudah kita pelajari, sedikit dong tentunya,. Berapalah materi yg berhubungan dengan respon Imun tu..
Maka dari itu aku Posting nih artikel yg mengarah ke Daftar Penyakit, tapi mohon maaf sebelumnya kalau artikel ini saya Kutip dari Situs Luar negeri, kenapa Luar Negeri, kalau di Negeri kita tercinta ini , bukannya tidak ada, ada sih, tapi itu masih sama dengan judul yg sudah teman-teman semua klaim,,
kalau mau meng-Klaim silahkan, tidak juga tak apa, aku juga dak maksa Untung dak jugo, rugi apolagi lagi, aku juga dak mikir Laba/Rugi ,tapi aku bukan mikir untung/rugi seperti yg dilakukan seorang anak Akutansi, ataupun Ekonomi, yg aku lakukan disini hanya ingin berbagi, Karena Berbagi Itu indah, Tapi berbagi itu ada juga tidak Indah, Berbagi penyakit contohnya, emang situ mau berbagi penyakit , sebut saja penyakit menular, situ mau berbagi Kotoran, Nggak kan..? ya udah dari pada lama-lama baco nah, tengok dibawah, dak mau baco dak sudah, dak makso jugo, yg baco artikel nih be aku jugo dak akan tau mungkin dan yg pasti aku dak ngasih hak akses apapun terhadap artikel yg sudah aku buat, dak aku ijinkan kau nak Copy walaupun setitik artikel aku, ini karno sehuruf itu berharga di Website Ingat Artikel Itu itu Memiliki Hak Cipta, Baco UU Hak Cipta,.
Kalau mau, copy artikel nih Tulis di Hp be, kalau dak tu Kirim pesan pada fasilitas yg udah aku sediakan, Gunakanlah itu teman-teman, Doa dan Usaha, Jangan Lupa itu, Buka Faslitas "Ide dan Survey" Itu gunonyo aku buat tu teman-teman biak kalian itu biso kirim pesan, aku ado terus di website ni, Setiap senin-Jum'at mulai dari 20.00 - 23.00,- , kalau nak cepat di respon, karno kito ni bahas imun buka/kirim ke email : info@rwcmediaku.com , saran@rwcmediaku.com , atau sms ke nomor yg ado pada Bagian bawah website rwcmediaku.com PALING BAWAH SEKALI,
Berikut ini adalah daftar nama penyakit yg Insya allah berhubungan dengan Respon Imun, Puas-Puas lah baco, kalau dak puas dipuaskan dewek.,. karno itu bukan urusan aku lagi, aku cuman sharing be..
Ini kalau kau nak tengok aku tulis dari A - Z, Insya Allah, kato maher zein,
Name: |
Accepted/
| Type | Autoantibody | Notes |
Acute disseminated encephalomyelitis (ADEM) | Accepted | |||
Addison’s Disease | interferon omega; transglutaminase; aromatic acid carboxylase; GAD; HAI; 17 hydroxylase; 21 hydroxylase | |||
Agammaglobulinemia | IGHM; IGLL1: CD79A; CD79B; BLNK; LRRC8A | |||
Alopecia areata | Accepted | T-cells | ||
Amyotrophic Lateral Sclerosis | ||||
Ankylosing Spondylitis | Accepted | ANCA? | CD8; HLA-B27 | |
Antiphospholipid syndrome | Accepted | anti-cardiolipin;anti pyruvate dehydrogenase; β2 glycoprotein I; phosphatidylserine; anti apoH; Annexin A5 | HLA-DR7, HLA-B8, HLA-DR2, HLA-DR3 | |
Antisynthetase syndrome | ||||
Atopic allergy | I | |||
Atopic dermatitis | I | |||
Autoimmune aplastic anemia | ||||
Autoimmune cardiomyopathy | Accepted | |||
Autoimmune enteropathy | ||||
Autoimmune hemolytic anemia | Accepted | II | complement activation | |
Autoimmune hepatitis | Accepted | cell-mediated | anti-mitochondrial antibodies; ANA; anti-smooth muscle antibodies, LKM-1; soluble liver antigen | |
Autoimmune inner ear disease | Accepted | [10] | ||
Autoimmune lymphoproliferative syndrome | Accepted | TNFRSF6; defective Fas-CD95 apoptosis | ||
Autoimmune peripheral neuropathy | Accepted | |||
Autoimmune pancreatitis | Accepted | ANA; anti-lactoferrin antibodiesanti-carbonic anhydrase antibodies; rheumatoid factor | ||
Autoimmune polyendocrine syndrome | Accepted | Unknownormultiple | APS-1 see Addison’s Disease | |
Autoimmune progesterone dermatitis | Accepted | |||
Autoimmune thrombocytopenic purpura | Accepted | anti gpIIb-IIIa or 1b-IX | ||
Autoimmune urticaria | Accepted | [11] | ||
Autoimmune uveitis | Accepted | HLAB-27? | ||
Balo disease/Balo concentric sclerosis | ||||
Behçet’s disease | immune-mediated systemic vasculitis; linkage to HLA-B51 (HLA-B27); very different manifestations with ulcers as common symptom; also called Morbus Adamandiades-Behçet | |||
Berger’s disease | IgA (elevated in 50% of patients), IgA (in mesangial deposits on kidney biopsy) | |||
Bickerstaff’s encephalitis | Anti-GQ1b 2/3 patients | similar to Guillain-Barré syndrome | ||
Blau syndrome | overlaps both sarcoidosis and granuloma annulare | |||
Bullous pemphigoid | IgG autoantibodies targeting the type XVII collagen component of hemidesmosomes | |||
Cancer | ||||
Castleman’s disease | Over expression of IL-6 | |||
Celiac disease | Accepted | IV | Anti-tissue transglutaminase antibodies | HLA-DQ8 and DQ2.5 |
Chagas disease | Suspected | |||
Chronic inflammatory demyelinating polyneuropathy | Anti-ganglioside antibodies:anti-GM1, anti-GD1a, anti-GQ1b | similar to Guillain-Barré syndrome | ||
Chronic recurrent multifocal osteomyelitis | LPIN2, D18S60,similar to Majeed syndrome | |||
Chronic obstructive pulmonary disease | Suspected | |||
Churg-Strauss syndrome | p-ANCA | |||
Cicatricial pemphigoid | anti-BP-1, anti BP-2 | precipitates C3 | ||
Cogan syndrome | ||||
Cold agglutinin disease | Accepted | II | IgM | idiopathic or secondary to leukemia or infection |
Complement component 2 deficiency | ||||
Contact dermatitis | III | |||
Cranial arteritis | aka Temporal arteritis; involves giant cells | |||
CREST syndrome | Anti-centromere antibodies Anti-nuclear antibodies | |||
Crohns Disease (one of two types of idiopathic inflammatory bowel disease “IBD”) | Accepted | IV | Innate immunity; Th17; Th1; ATG16L1; CARD15;XBP1; | |
Cushing’s Syndrome | cortisol binding globulin? | |||
Cutaneous leukocytoclastic angiitis | neutrophils | |||
Dego’s disease | Vasculopathy | |||
Dercum’s disease | Suspected | Lipoid tissue. | ||
Dermatitis herpetiformis | IgA; anti-epidermal transglutaminase antibodies | |||
Dermatomyositis | Accepted | histidine-tRNA anti-signal_recognition_peptide Anti-Mi-2 Anti-Jo1.[21] | B- and T-cell perivascular inflammatory infiltrate on muscle biopsy | |
Diabetes mellitus type 1 | Accepted | IV | Glutamic acid decarboxylase antibodies (GADA), islet cell antibodies (ICA), and insulinoma-associated autoantibodies (IA-2), anti-insulin antibodies | |
Diffuse cutaneous systemic sclerosis | anti-nuclear antibodies, anti-centromere and anti-scl70/anti-topoisomerase antibodies | COL1A2 and TGF-β1 | ||
Dressler’s syndrome | myocardial neo-antigens formed as a result of the MI | |||
Drug-induced lupus | anti-histone | |||
Discoid lupus erythematosus | III | IL-2 and IFN-gamma> | ||
Eczema | LEKTI, SPINK5, filaggrin.,Brain-derived neurotrophic factor (BDNF) and Substance P.[26] | |||
Endometriosis | Suspected[27] | |||
Enthesitis-related arthritis[28] | . | MMP3[29] TRLR2, TLR4,[30] ERAP1[31] | ||
Eosinophilic fasciitis | Accepted | |||
Eosinophilic gastroenteritis | IgE | IL-3, IL-5, GM-CSF, eotaxin | ||
Epidermolysis bullosa acquisita | COL7A1 | |||
Erythema nodosum | ||||
Erthroblastosis fetalis | II | ABO, Rh, Kell antibodies | mother’s immune system attacks fetus | |
Essential mixed cryoglobulinemia | ||||
Evan’s syndrome | ||||
Fibrodysplasia ossificans progressiva | ACVR1 Lymphocytes express increased BMP4 | |||
Fibrosing aveolitis aka Idiopathic_pulmonary_fibrosis | SFTPA1, SFTPA2, TERT, and TERC.[32] | |||
Gastritis | serum antiparietal and anti-IF antibodies | |||
Gastrointestinal pemphigoid | Accepted | |||
Giant cell arteritis | macrophage giant cells | |||
Glomerulonephritis | Sometimes | IgA | see Buerger’s Disease for IgA; Membranous glomerulonephritis for IgG; Membranoproliferative/mesangiocapillary GN (Complement activation); Goodpasture’s syndrome; Wegener’s granulomatosis | |
Goodpasture’s syndrome | Accepted | II | Anti-Basement Membrane Collagen Type IV Protein | |
Graves’ disease | Accepted | II | thyroid autoantibodies (TSHR-Ab) that activate the TSH-receptor (TSHR) | |
Guillain-Barré syndrome (GBS) | Accepted | IV | Anti-ganglioside | |
Hashimoto’s encephalopathy | Accepted | IV | alpha-enolase[33] | |
Hashimoto’s thyroiditis | Accepted | IV | antibodies against thyroid peroxidase and/or thyroglobulin | HLADR5, CTLA-4 |
Henoch-Schonlein purpura | immunoglobulin A (IgA) and complement component 3 (C3) | |||
Herpes gestationis aka Gestational Pemphigoid | IgG and C3 misdirected antibodies intended to protect the placenta | |||
Hidradenitis suppurativa | Suspected | |||
Hypogammaglobulinemia | IGHM, IGLL1, CD79A, BLNK, LRRC8A, CD79B | |||
Idiopathic Inflammatory Demyelinating Diseases | a variant of multiple sclerosis | |||
Idiopathic pulmonary fibrosis | SFTPA1, SFTPA2, TERT, and TERC.[32] | |||
Idiopathic thrombocytopenic purpura (See Autoimmune thrombocytopenic purpura) | Accepted | II | glycoproteins IIb-IIIa or Ib-IX, immunoglobulin G | |
IgA nephropathy | III? | IgA produced from marrow rather than MALT | ||
Inclusion body myositis | similar to polymyositis but does not respond to steroid therapy-activated T8 cells | |||
Chronic inflammatory demyelinating polyneuropathy | anti-ganglioside antibodies | similar to Guillain–Barré syndrome | ||
Interstitial cystitis | Suspected | Mast cells | ||
Juvenile idiopathic arthritis aka Juvenile rheumatoid arthritis | inconsistent ANA Rheumatoid_factor | |||
Kawasaki’s Disease | Suspected | ITPKC HLA-B51 | ||
Lambert-Eaton myasthenic syndrome | voltage-gated calcium channels; Q-type_calcium_channel, synaptogagmin, muscarinic acetylcholine receptor M1 | HLA-DR3-B8 | ||
Leukocytoclastic vasculitis | ||||
Lichen planus | ||||
Lichen sclerosus | ||||
Linear IgA disease (LAD) | ||||
Lou Gehrig’s disease (Also Amyotrophic lateral sclerosis) | VCP, ATXN2, OPTN, FIG4, TARDBP, ANG, VAPB, FUS, SETX, ALS2, SOD1 | |||
Lupoid hepatitis aka Autoimmune_hepatitis | ANA and SMA, LKM-1 , LKM-2 or LKM-3; antibodies against soluble liver antigen[37][38](anti-SLA, anti-LP) no autoantibodies detected (~20%) | |||
Lupus erythematosus | Accepted | III | Anti-nuclear antibodies[39] anti-Ro.[40] Also, they are often present in Sjögren’s syndrome.[41][42] | |
Majeed syndrome | LPIN2 | |||
Ménière’s disease | III | major peripheral myelin protein P0 | ||
Microscopic polyangiitis | p-ANCA myeloperoxidase | binds to neutrophils causing them to degranulate and damages endothelium | ||
Miller-Fisher syndrome see Guillain-Barre_Syndrome | Accepted | anti-GQ1b | ||
Mixed Connective Tissue Disease | Accepted[4] | anti-nuclear antibody anti-U1-RNP | HLA-DR4 | |
Morphea | Suspected[44] | |||
Mucha-Habermann disease aka Pityriasis_lichenoides_et_varioliformis_acuta | T-cells | |||
Multiple sclerosis | Suspected | IV | PECAM-1[45] Anti-Myelin Basic Protein | |
Myasthenia gravis | Accepted | II | nicotinic_acetylcholine_receptor MuSK_protein | HA-B8 HLA-DR3 HLA-DR1 |
Myositis | see Dermatomyositis and Polymyositis see Inclusion-body-myositis | |||
Narcolepsy[46][47] | Suspected | II | hypocretin or orexin | HLA-DQB1*0602 |
Neuromyelitis optica (Also Devic’s Disease) | II | NMO-IgG aquaporin 4. | ||
Neuromyotonia | Suspected | II | voltage-gated potassium channels. | |
Occular cicatricial pemphigoid | II? | BP-1, BP-2 | C3 deposition | |
Opsoclonus myoclonus syndrome | Suspected | IV? | Lymphocyte recruitment to CSF[54] | |
Ord’s thyroiditis | ||||
Palindromic rheumatism | anti-cyclic citrullinated peptide antibodies (anti-CCP) and antikeratin antibodies (AKA) | |||
PANDAS (pediatric autoimmune neuropsychiatric disorders associated with streptococcus) | Suspected | II? | antibodies against streptococcal infection serve as auto-antibodies | |
Paraneoplastic cerebellar degeneration | IV? II? | anti-Yo[57] (anti-cdr-2[58] in purkinje fibers) anti-Hu, anti-Tr, antiglutamate receptor | ||
Paroxysmal nocturnal hemoglobinuria (PNH) | Sometimes | complement attacks RBCs | ||
Parry Romberg syndrome | ANA | |||
Parsonnage-Turner syndrome | ||||
Pars planitis | ||||
Pemphigus vulgaris | Accepted | II | Anti-Desmoglein 3 | |
Pernicious anaemia | Accepted | II | anti-parietal cell antibody | |
Perivenous encephalomyelitis | ||||
POEMS syndrome | interleukin 1β, interleukin 6 and TNFα. vascular endothelial growth factor (VEGF), given the .[60] | |||
Polyarteritis nodosa | ||||
Polymyalgia rheumatica | ||||
Polymyositis | Accepted | IFN-gamma, IL-1, TNF-alpha | ||
Primary biliary cirrhosis | Accepted[62] | Anti-p62, Anti-sp100, Anti-Mitochondrial(M2)Anti-Ro aka SSA.[63] Also, they are often present in Sjögren’s syndrome | ||
Primary sclerosing cholangitis | overlap with primary biliary cirrhosis? | |||
Progressive inflammatory neuropathy | Suspected | |||
Psoriasis | Accepted | IV? | CD-8 T-cells, HLA-Cw6, IL-12b, IL-23b, TNFalpha, nfKb | |
Psoriatic arthritis | Accepted | IV? | HLA=B27 | |
Pyoderma gangrenosum | Can occur in conjunction with other immune-related disorders | |||
Pure red cell aplasia | ||||
Rasmussen’s encephalitis | anti-NR2A antibodies | |||
Raynaud phenomenon | Suspected | Can occur in conjunction with other immune-related disorders | ||
Relapsing polychondritis | Accepted | |||
Reiter’s syndrome | ||||
Restless leg syndrome | Suspected | May occur in Sjögren’s syndrome, celiac disease, and rheumatoid arthritis or in derangements of iron metabolism | ||
Retroperitoneal fibrosis | ||||
Rheumatoid arthritis | Accepted | III | Rheumatoid factor (anti-IgGFc), Anti-MCV , ACPAs(Vimentin | HLA-DR4, PTPN22, depleted B cells, TNF alpha, IL-17, (also maybe IL-1, 6, and 15) |
Rheumatic_fever | II | streptococcal M protein cross reacts with human myosin,[69]anti-DNase B, ASO | ||
Sarcoidosis | Suspected | IV | BTNL2; HLA-B7-DR15; HLA DR3-DQ2.[72] | |
Schizophrenia | Suspected | |||
Schmidt syndrome another form of APS | anti-21 hydroxylase, anti-17 hydroxylase | DQ2, DQ8 and DRB1*0404 | ||
Schnitzler syndrome | IgM? | |||
Scleritis | ||||
Scleroderma | Suspected | IV? | Scl-70 Anti-topoisomerase | dysregulated apoptosis? |
Serum Sickness | III | |||
Sjögren’s syndrome | Accepted | Anti-ro. Also, they are often present in Sjögren’s syndrome. | ||
Spondyloarthropathy | HLA-B27 | |||
Still’s disease see Juvenile Rheumatoid Arthritis | ANA | macrophage migration inhibitory factor[80] | ||
Stiff person syndrome | Suspected | glutamic acid decarboxylase (GAD), | GLRA1 (glycine receptor | |
Subacute bacterial endocarditis (SBE) | III | essential mixed cryoglobulinemia | ||
Susac’s syndrome | ||||
Sweet’s syndrome | GCSF | |||
Sydenham chorea see PANDAS | ||||
Sympathetic ophthalmia | ocular antigens following trauma | |||
Systemic lupus erythematosis see Lupus erythematosis | III | |||
Takayasu’s arteritis | ||||
Temporal arteritis (also known as “giant cell arteritis”) | Accepted | IV | ||
Thrombocytopenia | II | glycoproteins IIb-IIIa or Ib-IX in ITP anti-ADAMTS13 in TTP.[83]and HUS anti-cardiolipin (anti-cardiolipin antibodies) and β2glycoprotein I in Antiphospholipid syndrome anti-HPA-1a, anti-HPA-5b, and others in NAIT | multiple mechanisms | |
Tolosa-Hunt syndrome | ||||
Transverse myelitis | Accepted | Transverse Myelitis is a rare neurological disorder that is part of a spectrum of neuroimmunologic diseases of the central nervous system.http://www.myelitis.org/ | ||
Ulcerative colitis (one of two types of idiopathic inflammatory bowel disease “IBD”) | Accepted | IV | ||
Undifferentiated connective tissue disease different from Mixed connective tissue disease | Accepted | anti-nuclear antibody | HLA-DR4 | |
Undifferentiated spondyloarthropathy | ||||
Urticarial vasculitis | II? | anti C1q antibodies | clinically may resemble type I hypersensitivity! | |
Vasculitis | Accepted | III | sometimes ANCA | |
Vitiligo | Suspected | NALP-1 RERE, PTPN22, LPP, IL2RA, GZMB, UBASH3A and C1QTNF6 | ||
Wegener’s granulomatosis | Accepted | Anti-neutrophil cytoplasmic(cANCA) |
TERIMA KASIH
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