Amyloidogenic transthyretin amyloidosis Report
Amyloidogenic transthyretin amyloidosis
The gene mutations underlying this condition cause an abnormal intratissue deposition of altered proteins, which tend to form insoluble aggregates. These deposits mainly affect the cerebral and cardiac compartments, causing serious organ malfunctions.
More than 4 genes analyzed
It is recommended if:
This test is indicated for those with clinical suspicion of Amyloidogenic transthyretin amyloidosis or with a positive family history of the disease, to confirm the diagnosis or to know the personal genetic and transmission risk.
List of main conditions:
- Hypertrophic Cardiomyopathy
- Amyloidosis, Hereditary, Transthyretin-Related
Simple workflow
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