 | standing. In AL amyloidosis, specific indicators can include enlargement of the tongue and periorbital purpura. In wild-type ATTR amyloidosis, non-cardiac... 55 KB (5,432 words) - 21:07, 18 April 2024 |
 | Cardiac amyloidosis is a subcategory of amyloidosis where there is depositing of the protein amyloid in the cardiac muscle and surrounding tissues. Amyloid... 30 KB (3,368 words) - 04:03, 12 February 2024 |
AA amyloidosis is a form of amyloidosis, a disease characterized by the abnormal deposition of fibers of insoluble protein in the extracellular space of... 17 KB (1,590 words) - 20:58, 6 May 2024 |
Amyloid light-chain (AL) amyloidosis, also known as primary amyloidosis, is the most common form of systemic amyloidosis. The disease is caused when a... 11 KB (949 words) - 04:18, 19 April 2024 |
 | Amyloid (redirect from Hereditary amyloidosis) Edison J, Baethge BA, Jacobson DR (10 October 2018). "Amyloidosis: Definition of Amyloid and Amyloidosis, Classification Systems, Systemic Amyloidoses". Medscape... 60 KB (6,514 words) - 10:39, 27 March 2024 |
Wild-type transthyretin amyloid (redirect from Senile systemic amyloidosis) marker of cardiac amyloidosis. A much better survival has been reported for patients with WTTA as opposed to cardiac AL amyloidosis. The condition is... 10 KB (1,240 words) - 00:53, 29 November 2023 |
 | Primary cutaneous amyloidosis is a form of amyloidosis associated with oncostatin M receptor. This type of amyloidosis has been divided into the following... 4 KB (260 words) - 23:33, 10 July 2022 |
 | X-linked reticulate pigmentary disorder (redirect from Partington amyloidosis) PJ, Prentice RS, Cavaglia A, Simpson NE (1981). "Familial cutaneous amyloidosis with systemic manifestations in males". American Journal of Medical Genetics... 10 KB (886 words) - 20:01, 2 January 2024 |
 | Muckle–Wells syndrome (redirect from Urticaria-deafness-amyloidosis) which causes sensorineural deafness and recurrent hives, and can lead to amyloidosis. Individuals with MWS often have episodic fever, chills, and joint pain... 6 KB (553 words) - 13:09, 9 January 2024 |
 | LECT2 Amyloidosis (ALECT2) is a form of amyloidosis caused by the LECT2 protein. It was found to be the third most common (~3% of total) cause of amyloidosis... 17 KB (2,114 words) - 16:01, 30 March 2024 |
 | polyneuropathy, as well as wild-type transthyretin amyloidosis, which formerly was called senile systemic amyloidosis. It works by stabilizing the quaternary structure... 19 KB (1,571 words) - 19:18, 23 April 2024 |
Plasma cell dyscrasias (section Amyloidosis) heavy chain amyloidosis (AH amyloidosis) in which amyloid deposits contain only free heavy chains. The deposits in a third type, AHL amyloidosis, consists... 81 KB (10,827 words) - 12:54, 14 March 2024 |
| Familial renal amyloidosis is a form of amyloidosis primarily presenting in the kidney. It is associated most commonly with congenital mutations in the... 5 KB (405 words) - 12:46, 15 February 2024 |
 | Proteinopathy (category Amyloidosis) by a similar mechanism, including Aβ amyloidosis, amyloid A (AA) amyloidosis, and apolipoprotein AII amyloidosis, tauopathy, synucleinopathy, and the... 62 KB (4,592 words) - 03:35, 12 May 2024 |
| Familial amyloid polyneuropathy (redirect from Systemic senile amyloidosis) polyneuropathy, also called transthyretin-related hereditary amyloidosis, transthyretin amyloidosis abbreviated also as ATTR (hereditary form), or Corino de... 14 KB (1,486 words) - 16:53, 7 February 2024 |
Heredofamilial amyloidosis is an inherited condition that may be characterized by systemic or localized deposition of amyloid in body tissues.: 522 Amyloidosis List... 1 KB (76 words) - 18:15, 12 October 2023 |
immunoglobulin-induced renal amyloidosis (e.g. AL amyloidosis) represented 86% of the cases). Hereditary fibrinogen Aα-Chain amyloidosis is, however, the most... 31 KB (3,248 words) - 09:07, 18 February 2024 |
Haemodialysis-associated amyloidosis is a form of systemic amyloidosis associated with chronic kidney failure. Amyloidosis is the accumulation of misfolded... 5 KB (411 words) - 20:13, 29 February 2024 |
 | amyloid diseases including wild-type transthyretin amyloidosis, hereditary transthyretin amyloidosis, familial amyloid polyneuropathy (FAP), and familial... 20 KB (2,382 words) - 16:13, 22 January 2024 |
 | seen in nonsecretory multiple myeloma and amyloid light chain amyloidosis (AL amyloidosis). The Bence Jones protein was described by the English physician... 6 KB (607 words) - 08:18, 18 January 2024 |
| Familial Amyloidosis, Finnish Type (FAF), also called hereditary gelsolin amyloidosis and AGel amyloidosis (AGel), is an amyloid condition with a number... 8 KB (722 words) - 23:14, 3 November 2023 |
 | fossa. Raccoon eyes may also be a sign of disseminated neuroblastoma, amyloidosis, Kaposi’s sarcoma or multiple myeloma. It also can be temporary result... 4 KB (380 words) - 09:55, 17 February 2024 |
 | Serum amyloid P component (section In amyloidosis) Pedro Pinho e. (eds.). Amyloid and amyloidosis: proceedings of the Third International Symposium on Amyloidosis, Póvoa de Varzim, Portugal, 23–28 September... 6 KB (744 words) - 11:38, 20 October 2023 |
 | Meninges (redirect from Leptomeningeal amyloidosis) In anatomy, the meninges (/məˈnɪndʒiːz/, sg.: meninx (/ˈmiːnɪŋks/ or /ˈmɛnɪŋks/), from Ancient Greek μῆνιγξ (mēninx) 'membrane') are the three membranes... 14 KB (1,584 words) - 15:16, 2 May 2024 |
 | Lattice corneal dystrophy (redirect from Finnish type amyloidosis) to chromosome 5q. type II or Finnish type amyloidosis: associated with manifestations of systemic amyloidosis due to accumulation of gelsolin. Associated... 8 KB (849 words) - 23:18, 20 September 2022 |
Eplontersen (category Amyloidosis) transthyretin-mediated amyloidosis. It is a transthyretin-directed antisense oligonucleotide. It was developed to treat hereditary transthyretin amyloidosis by Ionis... 11 KB (473 words) - 19:54, 5 April 2024 |
 | biggest risk factors for spontaneous bleeding are high blood pressure and amyloidosis. Other risk factors include alcoholism, low cholesterol, blood thinners... 44 KB (4,483 words) - 13:03, 4 May 2024 |
English footballer (Manchester City, Brighton, Sheffield Wednesday), amyloidosis. Tahnoun bin Mohammed Al Nahyan, 82, Emirati royal and politician, ruler's... 86 KB (6,315 words) - 03:57, 15 May 2024 |
 | hide as well as display other 'shy' behaviour. Familial renal amyloidosis or AA amyloidosis, a kidney disorder due to a mutation in the AA amyloid protein... 18 KB (1,960 words) - 20:42, 21 March 2024 |
FDA approval for the treatment of hereditary transthyretin-mediated amyloidosis in October 2018. The application for inotersen was granted orphan drug... 23 KB (2,212 words) - 22:18, 9 November 2023 |