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  2. AL amyloidosis - Wikipedia

    en.wikipedia.org/wiki/AL_amyloidosis

    Amyloid light-chain (AL) amyloidosis, also known as primary amyloidosis, is the most common form of systemic amyloidosis. [1] The disease is caused when a person's antibody-producing cells do not function properly and produce abnormal protein fibers made of components of antibodies called light chains. These light chains come together to form ...

  3. Amyloidosis - Wikipedia

    en.wikipedia.org/wiki/Amyloidosis

    Amyloidosis is a group of diseases in which abnormal proteins, known as amyloid fibrils, build up in tissue. [4] There are several non-specific and vague signs and symptoms associated with amyloidosis. [5] These include fatigue, peripheral edema, weight loss, shortness of breath, palpitations, and feeling faint with standing. [5]

  4. Amyloid cardiomyopathy - Wikipedia

    en.wikipedia.org/wiki/Amyloid_cardiomyopathy

    Chemotherapy can treat amyloidosis if it is related to immunoglobulins. [4] Liver transplant can treat amyloidosis if it is related to familial transthyretin. [4]Acoramidis (Attruby) was approved for medical use in the United States in November 2024, to treat adults with cardiomyopathy of wild-type or variant (hereditary) transthyretin-mediated amyloidosis (ATTR-CM) to reduce death and ...

  5. Amyloid - Wikipedia

    en.wikipedia.org/wiki/Amyloid

    To date, 37 human proteins have been found to form amyloid in pathology and be associated with well-defined diseases. [2] The International Society of Amyloidosis classifies amyloid fibrils and their associated diseases based upon associated proteins (for example ATTR is the group of diseases and associated fibrils formed by TTR). [3]

  6. Cardiac amyloidosis - Wikipedia

    en.wikipedia.org/wiki/Cardiac_amyloidosis

    The vast majority of familial cardiac amyloidosis still present after the age of 60. [4] A common mutation is the TTR gene mutation Val122Ile. [2] It is estimated that 3.5–4% of African Americans in The United States have the Val 122lle mutation. [4] This type of amyloidosis can be identified by genetic testing for protein mutation. [4]

  7. AA amyloidosis - Wikipedia

    en.wikipedia.org/wiki/AA_amyloidosis

    AA amyloidosis is a form of amyloidosis, a disease characterized by the abnormal deposition of fibers of insoluble protein in the extracellular space of various tissues and organs. In AA amyloidosis, the deposited protein is serum amyloid A protein (SAA), an acute-phase protein which is normally soluble and whose plasma concentration is highest ...

  8. Exclusive: Quizlet acquires Slader as it aims to become the ...

    www.aol.com/news/quizlet-schools-reopening...

    The company raised a $30 million Series C in May 2020, bringing the company's post-money valuation to $1 billion. In the U.S., Quizlet is used by two in three high school students and one in two ...

  9. Shoulder pad sign - Wikipedia

    en.wikipedia.org/wiki/Shoulder_pad_sign

    [1] [2] [3] This type of infiltration is not common, but it is pathognomonic for AL amyloidosis. [1] [2] [3] Analysis of the amyloid protein has demonstrated that it has a kappa III Ig light chain structure. [1] The variable region of kappa III amyloid proteins may show an increased likelihood of depositing in soft tissue. [1]