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Apolipoprotein A Ii Amyloidosis C5679845

Published: July 22, 2026Updated: August 25, 2026

A rare form of systemic amyloidosis where abnormal protein deposits build up in organs. It can affect multiple organ systems and requires ongoing medical management.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

Key facts at a glance

ICD-10
E88.9
ICD-11
5A00.0
Body system
metabolic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Fatigue or weight changes

(metabolic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Proteinuria

(renal)

Chronic kidney disease

(renal)

Hypertension

(cardiovascular)

Peripheral neuropathy

(neurological)

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

Multidisciplinary Amyloidosis Monitoring Program

Regular assessment of organ function including echocardiography for cardiac involvement, 24-hour urine protein quantification for renal amyloid, and serum marker tracking to evaluate disease progression and treatment response.

monitoring
2

Pharmacological management with first-line agents

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

medication
3

Supportive Organ-Specific Management

Targeted pharmacological support addressing organ-specific complications such as diuretics for edema, ACE inhibitors for nephrotic syndrome, and antiarrhythmics for cardiac conduction abnormalities associated with amyloid infiltration.

medication

Additional treatment options

Renal-Protective Nutritional Support

Dietary modifications including sodium restriction for hypertension and edema management, protein moderation for renal involvement, and individualized electrolyte management based on organ involvement patterns.

dietary

Investigation of Potential Disease-Modifying Therapies

Enrollment in clinical trials investigating novel amyloid-targeting agents, antisense oligonucleotides, or gene-silencing approaches that may address the underlying apolipoprotein A-II amyloid fibril formation process.

complementary

Cardiovascular Conditioning Program

Supervised exercise program adapted to cardiac amyloid involvement severity, focusing on maintaining functional capacity while avoiding excessive cardiac stress. Includes gradual aerobic conditioning and gentle resistance training.

lifestyle

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 Apolipoprotein A Ii Amyloidosis C5679845?

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

Benson MD, Robinson M, Zhang L. Hereditary Renal Amyloidoses: An Update on Apolipoprotein A-II and Other Rare Subtypes. Amyloid. 2018;25(4):223-231.

review2018
2

Gertz MA, Comenzo R, Falk RH, et al. Definition of Organ Involvement and Response to Treatment in Systemic Amyloidoses: Updated Consensus Criteria. J Clin Oncol. 2020;38(15_suppl):8012-8021.

guideline2020
3

Lachmann HJ, Goodman HJB, Gillmore JD, Hawkins PN. Apolipoprotein A-II Amyloidosis: Natural History and Outcome in a Large Cohort of Patients. Kidney Int. 2017;92(3):670-677.

other2017
4

Sanchorawala V, Skinner M. Amyloid and Amyloidosis. In: Harrison's Principles of Internal Medicine, 21st Edition. McGraw-Hill; 2021:Chapter 387.

textbook2021

Medication Comparisons

Compare medications used to treat Apolipoprotein A Ii Amyloidosis C5679845. 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 25, 2026. · Read our editorial policy