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3,180 Possible Causes for Amyloidosis, V

  • Dementia

    Livingston, G ; Sommerlad, A ; Orgeta, V ; Costafreda, SG ; Huntley, J ; Ames, D ; Ballard, C ; ...[] Local amyloidosis is known to occur in the atrophic form of general paresis.[] Yazici H, Yurdakul S, Hamuryudan V: Behcet disease . Curr Opin Rheumatol 2001, 13: 18–22. PubMed CrossRef Google Scholar 56.[]

  • Osteoporosis

    Google Scholar Medline ISI Pettilä V , Leinonen P , Markkola A , Hiilesmaa V , Kaaja R .[] Systemic diseases such as amyloidosis and sarcoidosis can also lead to osteoporosis. Renal insufficiency can lead to renal osteodystrophy.[] V.[]

  • Cryopyrin-Associated Periodic Syndrome

    Neurological involvement was less strongly associated with V198M, E311 K and A439 V alleles.[] She was diagnosed with renal amyloidosis at 32 years of age.[] Cartault F , Caux F , Chevrant-Breton J , Cordier MP , Dhote R , Duquesne A , Frances C , Frange P , Gaillard D , Granel B , Grateau G , Hachulla E , Hatron PY , Hentgen V[]

  • Amyloidosis

    The clinical progress and treatment response measured by serial factor V levels and coagulation parameters was then prospectively tracked.[] The full pathophysiological pathway of the amyloidosis is however dependent on the type of amyloidosis. There is no clear method of preventing amyloidosis.[] Park KI, Ourednik J, Ourednik V, et al. Global gene and cell replacement strategies via stem cells. Gene Ther. 2002;9:613-24. Rocken C, Shakespeare A.[]

  • Tumor Necrosis Factor Receptor 1-associated Periodic Syndrome

    V. Rameev, V. V. and Kozlovskaya, L. V. 2017. Autoinflammatory diseases and kidney involvement. Terapevticheskii arkhiv , Vol. 89, Issue. 6, p. 4.[] Urinary protein analysis helps to monitor evolution of renal amyloidosis. Mutational analyses can help confirm the diagnosis.[] External links [ edit ] PubMed v t e Cell surface receptor deficiencies G protein-coupled receptor (including hormone ) Class A TSHR ( Congenital hypothyroidism 1 ) LHCGR[]

  • Familial Mediterranean Fever

    Genetic analysis demonstrated M694 V mutation (one homozygous and the other heterozygous) in both of the patients.[] Abstract Amyloidosis cutis dyschromica is a rare type of primary cutaneous amyloidosis characterized by reticulate hyper-pigmentation with discrete hypopigmented macules.[] Giaglis S, Papadopoulos V, Kambas K, Doumas M, Tsironidou V, Rafail S, Kartalis G, Speletas M, Ritis K (2007) MEFV alterations and population genetics analysis in a large[]

  • Heart Failure

    , Tseluyko V , Vatutin M , Voronkov L , Yagensky A , Zabgorodni A , Zheleznyy V , Zhurba S , Reshtoko D , Dyadyk O , Vizir V , Faynyk A , Kaydashev I , Dolzhenko M , Perseva[] Abstract Cardiac amyloidosis may occur in any type of systemic amyloidosis. The clinical picture is often characterized by restrictive cardiomyopathy.[] Cardiac MRI showed biventricular late gadolinium enhancement, and endomyocardial biopsy confirmed monoclonal immunoglobulin light-chain (AL) amyloidosis.[]

  • Primary Amyloidosis

    Kumar and Taxiarchis V.[] […] systemic amyloidosis.[] Gloro, V. Rouleau and P. Rousselot , Amylose hépatique , EMC - Hépatologie , 1 , 1 , (1) , (2006) . P. Campbell and C.[]

  • TTR Amyloidosis with Polyneuropathy

    Coelho T, Maia LF, Silva AM, Cruz MW, Planté-Bordeneuve V, Suhr OB et al.[] […] and leptomeningeal TTR amyloidosis.[] Suhr Evolving landscape in the management of transthyretin amyloidosis [2] V. Planté-Bordeneuve, G. Said Familial amyloid polyneuropathy [3] V.[]

  • Primary Myelofibrosis

    Campanelli R 1 , Fois G 1 , Catarsi P 1 , Poletto V 1 , Villani L 1 , Erba BG 2 , Maddaluno L 2 , Jemos B 3 , Salmoiraghi S 4 , Guglielmelli P 5 , Abbonante V 6, 7 , Di Buduo[] Abnormalities of humoral immunity: variety of autoantibodies and circulating immune complexes may be detected and amyloidosis may develop.[] A variety of autoantibodies and circulating immune complexes may be detected, and amyloidosis may develop.[]

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