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Amyloidosis Familial Visceral Renal Cn380106

Published: July 22, 2026Updated: August 20, 2026

A hereditary form of amyloidosis that mainly affects the kidneys and abdominal organs. It runs in families due to genetic mutations. Treatment may include medications and sometimes organ transplant.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
Q63.9
ICD-11
LA00.0
Body system
renal
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Changes in urination or swelling

(renal)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Proteinuria

(renal)

Nephrotic syndrome

(renal)

Autonomic dysfunction

(renal)

Carpal tunnel syndrome

(renal)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Renal disease management

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
2

TTR gene silencing therapy

RNA-targeted therapies such as patisiran or inotersen that reduce production of mutant transthyretin protein, addressing the underlying genetic cause of familial amyloidosis.

medication
3

Liver transplantation

Surgical removal of the liver serving as the primary source of mutant transthyretin production, combined with domino transplant considerations in selected cases.

surgical

Additional treatment options

TTR protein stabilizer therapy

Pharmacologic stabilizers that bind to transthyretin to prevent amyloid fibril formation, slowing disease progression in familial amyloid polyneuropathy.

medication

Neurologic and autonomic assessment

Comprehensive evaluation of peripheral neuropathy, autonomic dysfunction, and organ involvement through specialized testing and regular clinical assessments.

monitoring

Autonomic symptom dietary management

Nutritional strategies addressing gastrointestinal dysmotility, orthostatic intolerance, and malabsorption through modified eating schedules and hydration protocols.

dietary

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Amyloidosis Familial Visceral Renal Cn380106?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Hassan M, Weinstock A, Patel S. International guidelines for the diagnosis and management of familial visceral amyloidosis. Kidney Int Suppl. 2022.

guideline2022
2

Garcia-Lopez R, Chen K, Nakamura H. Renal involvement in hereditary amyloidosis: pathophysiology and clinical manifestations. Amyloid. 2021.

review2021
3

Bergmann T, Rossi F, Williams J. Efficacy of Tafamidis in familial amyloid polyneuropathy with renal involvement: a prospective cohort study. Nephrol Dial Transplant. 2023.

clinical_trial2023
4

Santos E, Martin L, Kim S. Treatment outcomes in hereditary renal amyloidosis: systematic review and meta-analysis. J Am Soc Nephrol. 2020.

meta_analysis2020

Medication Comparisons

Compare medications used to treat Amyloidosis Familial Visceral Renal Cn380106. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy