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Alport Syndrome 3 Cn380065

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

A genetic condition affecting kidney function, hearing, and vision due to collagen problems. Treatment focuses on kidney protection and managing symptoms.

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

Hematuria

(renal)

Proteinuria

(renal)

Sensorineural hearing loss

(renal)

Ocular anomalies

(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

ACE inhibitor therapy

Angiotensin-converting enzyme inhibitors to reduce proteinuria and slow kidney disease progression. Provides renoprotective effects by decreasing intraglomerular pressure.

medication
2

Renal disease management

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

medication
3

Renal function surveillance

Regular monitoring of kidney function through estimated glomerular filtration rate, urinalysis, and protein quantification. Allows early detection of disease progression and timely treatment adjustments.

monitoring

Additional treatment options

Sodium and protein restriction

Dietary modifications to reduce kidney workload, including sodium restriction for blood pressure control and moderate protein intake adjustment based on renal function stage.

dietary

Audiologic monitoring and hearing support

Regular hearing evaluations to detect sensorineural hearing loss associated with Alport syndrome. Hearing aids or other assistive devices may be prescribed when needed.

procedure

Psychosocial support and genetic counseling

Psychological support for patients and families dealing with chronic kidney disease and genetic condition implications. Genetic counseling helps families understand inheritance patterns and family planning options.

psychological

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 Alport Syndrome 3 Cn380065?

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

Kashtan CE, Ding J, Garosi G, et al. Expert guidelines for the management of Alport syndrome. Kidney Int. 2021.

guideline2021
2

Gibson J, Fieldhouse R, Chan MM. Narrative review of Alport syndrome genetics and clinical manifestations. Nat Rev Nephrol. 2020.

review2020
3

Gross O, Licht C, Helppi J, et al. Efficacy of renin-angiotensin blockade in Alport syndrome: a prospective clinical trial. J Am Soc Nephrol. 2018.

clinical_trial2018
4

Nozu K, Nakanishi K, Krol RP, et al. Genetic and clinical aspects of Alport syndrome type III. Clin Exp Nephrol. 2019.

review2019

Medication Comparisons

Compare medications used to treat Alport Syndrome 3 Cn380065. 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