Hereditary amyloidosis is a rare genetic disease characterized by abnormal protein deposits in organs, leading to symptoms like fatigue, heart issues, nerve problems, and kidney dysfunction. Early recognition of these signs is crucial for timely management and improved outcomes.

Hereditary amyloidosis is a rare genetic disorder caused by abnormal protein deposits called amyloids accumulating in various organs. These deposits can form in different tissues, leading to a range of symptoms that vary based on their location and severity. Early detection of these signs can facilitate prompt diagnosis and treatment. Common symptoms include extreme fatigue, unintended weight loss, skin color changes, bloating, anemia, joint pain, shortness of breath, tongue swelling, weak grip, and tingling in extremities. When the heart is involved, symptoms such as chest discomfort, irregular heartbeat, and swelling may occur. Nerve-related issues like numbness, burning sensations, and autonomic dysfunction can also arise. Gastrointestinal disturbances like nausea and diarrhea, along with kidney problems such as swelling and proteinuria, are additional indicators of this condition.