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Alg8 Related Autosomal Dominant Polycystic Kidney And Or Liver Disease Cn379637

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

An inherited condition causing fluid-filled cysts in kidneys and sometimes the liver. Treatment focuses on managing complications and preserving organ function.

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
moderate
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Changes in urination or swelling

(renal)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Hypertension

(renal)

Flank pain

(renal)

Hematuria

(renal)

Hepatic cyst formation

(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

Multisystem Imaging Surveillance

Regular imaging of kidneys and liver through ultrasound, CT, or MRI to monitor cyst growth and organ function. Blood tests assess kidney and liver function markers periodically to detect changes early.

monitoring
2

Renal disease management

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
3

Blood Pressure Management

Use of antihypertensive medications to control blood pressure and protect kidney function. ACE inhibitors or ARBs are commonly used as they may slow cyst progression and provide renal protection.

medication

Additional treatment options

Cyst Decompression Procedures

Surgical interventions to drain or remove problematic cysts causing pain, bleeding, or organ compression. Options include laparoscopic cyst decortication or more extensive surgical approaches depending on cyst location and severity.

surgical

Renal-Protective Diet

Dietary modifications including reduced sodium intake, moderate protein consumption, and adequate hydration. These changes help manage blood pressure and reduce kidney strain while maintaining nutritional balance.

dietary

Activity and Pain Management

Regular low-impact exercise to maintain cardiovascular health while managing abdominal discomfort. Heat therapy, gentle stretching, and activity pacing help manage symptoms during cyst-related pain episodes.

lifestyle

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Alg8 Related Autosomal Dominant Polycystic Kidney And Or Liver Disease Cn379637?

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

Cornec-Le Gall E, Audrezet MP, Le Meur Y. Genetics of autosomal dominant polycystic kidney disease: clinical implications. Nephrol Dial Transplant. 2022.

review2022
2

Chapman AB, Devuyst O, Eckardt KU, et al. Autosomal dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) controversies conference. Kidney Int. 2015.

guideline2015
3

Gevers TJ, Drenth JP. Diagnosis and management of polycystic liver disease. Nat Rev Gastroenterol Hepatol. 2013.

review2013
4

Besse W, Dong K, Choi J, et al. Polycystic kidney disease genes: insights from rare variants and population studies. Clin J Am Soc Nephrol. 2021.

other2021

Medication Comparisons

Compare medications used to treat Alg8 Related Autosomal Dominant Polycystic Kidney And Or Liver Disease Cn379637. 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