Systemic ATTR-amyloidosis, a Rare Form of Internal Organ Damage
نویسندگان
چکیده
منابع مشابه
Amyloidosis cutis dyschromia: a rare form of primary cutaneous amyloidosis.
Amyloidosis cutis dyschromia is a rare form of primary cutaneous amyloidosis. Amyloid deposition in the skin occurs without systemic manifestations and produces hypopigmented and hyperpigmented macules. A 19-year-old woman is presented with progression of this condition over 16 years.
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Methods As part of a protocolised model of care involving comprehensive annual clinical evaluation (including DPD scintigraphy, echocardiography, ECG, neurological testing, cardiac magnetic resonance imaging (CMR), 6-minute walk test and blood tests), patients completed the KCCQ and SF-36 questionnaires. The KCCQ quantifies physical function (PF), symptoms, social function (SF), and QoL in card...
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Systemic amyloidosis related to mutation of TTR gene can be complicated with Familial Amyloid Cardiomyopathy (TTR-FAC), a severe and life threatening form of heart failure with preserved ejection fraction, with a poor prognosis. To date there is no proven effective specific treatment against TTR-FAC, and the usual treatments of chronic heart failure are either ineffective or contra indicated, e...
متن کاملFirst European Congress on Hereditary ATTR amyloidosis.
Familial amyloidosis typically causes a nerve length-dependent small fiber polyneuropathy that starts in the feet with loss of temperature and pain sensations, associated with autonomic dysfunction, which can be extremely severe and life threatening. Neuropathic pain is commonly associated with amyloid neuropathy. There are no randomized controlled trials in peripheral neuropathies specifically...
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ژورنال
عنوان ژورنال: Rational Pharmacotherapy in Cardiology
سال: 2019
ISSN: 2225-3653,1819-6446
DOI: 10.20996/1819-6446-2019-15-3-349-358