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  2. Proteinopathy - Wikipedia

    en.wikipedia.org/wiki/Proteinopathy

    In medicine, proteinopathy ([pref. protein]; -pathy [suff. disease]; proteinopathies pl.; proteinopathic adj), or proteopathy, protein conformational disorder, or protein misfolding disease, is a class of diseases in which certain proteins become structurally abnormal, and thereby disrupt the function of cells, tissues and organs of the body ...

  3. Limbic-predominant age-related TDP-43 encephalopathy

    en.wikipedia.org/wiki/Limbic-predominant_age...

    LATE often coexists with a small blood vessel pathology affecting cerebral arterioles, which is termed arteriolosclerosis. [53] LATE is more common in cases with comorbid tauopathy, including Alzheimer's-type plaques and tangles, primary age-related tauopathy (PART), and age-related tau astrogliopathy. [2] [5] [6]

  4. Hereditary inclusion body myopathy - Wikipedia

    en.wikipedia.org/wiki/Hereditary_inclusion_body...

    Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (IBMPFD), now more commonly referred to as multisystem proteinopathy (MSP), is an autosomal dominant condition caused by mutations in VCP, HNRPA2B1 or HNRNPA1; it is a multisystem degenerative disorder that can affect muscle, bone, and/or the central nervous system.

  5. Serum protein electrophoresis - Wikipedia

    en.wikipedia.org/wiki/Serum_protein_electrophoresis

    Serum protein electrophoresis (SPEP or SPE) is a laboratory test that examines specific proteins in the blood called globulins. [1] The most common indications for a serum protein electrophoresis test are to diagnose or monitor multiple myeloma , a monoclonal gammopathy of uncertain significance (MGUS), or further investigate a discrepancy ...

  6. Multisystem proteinopathy - Wikipedia

    en.wikipedia.org/wiki/Multisystem_proteinopathy

    Multisystem proteinopathy (MSP) is a dominantly inherited, pleiotropic, degenerative disorder of humans that can affect muscle, bone, and/or the central nervous system.MSP can manifest clinically as classical amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), inclusion body myopathy (IBM), Paget's disease of bone (PDB), or as a combination of these disorders. [1]

  7. Variably protease-sensitive prionopathy - Wikipedia

    en.wikipedia.org/wiki/Variably_protease...

    Variably protease-sensitive prionopathy (VPSPr) (formerly known as Protease Sensitive Prionopathy) is a sporadic prion protein disease first described in an abstract for a conference on prions in 2006, and this study was published in a 2008 report on 11 cases.

  8. Huntington's disease - Wikipedia

    en.wikipedia.org/wiki/Huntington's_disease

    The genetic test for HD consists of a blood test, which counts the numbers of CAG repeats in each of the HTT alleles. [65] Cutoffs are given as follows: At 40 or more CAG repeats, full penetrance allele (FPA) exists. [66] A "positive test" or "positive result" generally refers to this case. A positive result is not considered a diagnosis, since ...

  9. Pathophysiology - Wikipedia

    en.wikipedia.org/wiki/Pathophysiology

    The pathophysiology of hypertension is that of a chronic disease characterized by elevation of blood pressure. Hypertension can be classified by cause as either essential (also known as primary or idiopathic) or secondary. About 90–95% of hypertension is essential hypertension. [23] [24] [25] [26]