Transthyretin Methionine-30 Amyloidosis
📋Overview
Transthyretin Methionine-30 Amyloidosis is a hereditary form of transthyretin amyloidosis (ATTR amyloidosis) caused by a mutation substituting methionine at position 30 of the transthyretin (TTR) protein. It is a variant of hereditary ATTR amyloidosis, a condition characterized by abnormal amyloid protein deposits derived from mutated transthyretin, leading to progressive organ dysfunction, primarily affecting peripheral nerves and the heart.
Educational overview only. This page summarizes publicly available health information for general understanding and awareness. It does not provide medical advice, diagnosis, or treatment. For personalized guidance or care decisions, consult a qualified healthcare professional.
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