Hereditary Amyloidosis

Hereditary amyloidosis is a group of rare diseases of genetic origin in which an abnormal protein, called amyloid, deposits in different organs and alters their function.

Organs it can affect: Depending on the type, it can involve the heart, the nervous system, the kidneys, the digestive system or other tissues, so its manifestations are very varied.

Possible signs: They can include tingling or weakness, alterations in heart rhythm, swelling or digestive changes, which usually evolve progressively.

Which specialist treats it? Because of its multisystem nature, the evaluation usually involves the internist, the cardiologist, the neurologist and the nephrologist, who coordinate the necessary studies. Faced with persistent symptoms or a family history, it is advisable to seek a specialized evaluation.