Amyloidosis history and symptoms: Difference between revisions

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===Less Common Symptoms===
===Less Common Symptoms===
Less common symptoms of Amyloidosis include:
*[[Macroglossia|Enlarged tongue]]
*[[Macroglossia|Enlarged tongue]]
*[[Abdominal pain]]
*[[Abdominal pain]]

Revision as of 15:01, 30 October 2019

Amyloidosis Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Primary amyloidosis
Secondary amyloidosis
Familial amyloidosis
Wild-type (senile) amyloidosis
Cardiac amyloidosis
Beta-2 microglobulin related amyloidosis
Gelsolin related amyloidosis
Lysozyme amyloid related amyloidosis
Leucocyte cell-derived chemotaxin 2 related amyloidosis
Fibrinogen A alpha-chain associated amyloidosis

Pathophysiology

Causes

Differentiating Amyloidosis from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

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Treatment

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Case #1

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Shyam Patel [2]; Associate Editor(s)-in-Chief: Shaghayegh Habibi, M.D.[3]

Overview

In amyloidosis, the range of symptoms depends on specific tissues and organs involved. Symptoms can be quite diverse.

History and Symptoms

History

Patients with amyloidosis may have a positive history of:[1]

Common Symptoms

Common symptoms in patients with primary amyloidosis include:[1]

Less Common Symptoms

Less common symptoms of Amyloidosis include:

References

  1. 1.0 1.1 Mahmood S, Palladini G, Sanchorawala V, Wechalekar A (February 2014). "Update on treatment of light chain amyloidosis". Haematologica. 99 (2): 209–21. doi:10.3324/haematol.2013.087619. PMC 3912950. PMID 24497558.

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