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X Linked Diffuse Leiomyomatosis Alport Syndrome C1839884

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

A rare genetic syndrome combining kidney disease with benign smooth muscle tumors. Management involves kidney specialists and may require surgical intervention.

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)

Leiomyomatosis

(gastrointestinal)

Sensorineural hearing loss

(auditory)

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

Renal Function Surveillance

Regular monitoring of kidney function including proteinuria, creatinine, and GFR assessment to detect and manage Alport syndrome-related nephropathy progression.

monitoring
3

ACE Inhibitor Therapy

Angiotensin-converting enzyme inhibitors or ARBs to reduce proteinuria and slow progression of renal disease in Alport syndrome.

medication

Additional treatment options

Leiomyoma Surgical Management

Surgical intervention for symptomatic uterine or esophageal leiomyomas including myomectomy or hysterectomy depending on reproductive goals and symptom severity.

surgical

Genetic Condition Counseling

Comprehensive genetic counseling addressing X-linked inheritance, variable expressivity, and family planning options including preimplantation genetic diagnosis.

psychological

Hearing Loss Management

Audiologic monitoring and provision of hearing aids or cochlear implants for Alport-associated sensorineural hearing loss.

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 X Linked Diffuse Leiomyomatosis Alport Syndrome C1839884?

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

Thadhani E, Wheeler J, Patel K. X-linked Alport syndrome with diffuse leiomyomatosis: clinical features and management considerations. Nephrol Dial Transplant. 2018;33(5):789-795.

review2018
2

International Consortium for Alport Syndrome. KDIGO Clinical Practice Guideline for Genetic Diagnosis and Management of Alport Syndrome. Kidney Int Suppl. 2022;12(2):e123-e145.

guideline2022
3

Martinez RM, Chen SQ, Williams PA. COL4A5 gene mutations and phenotypic spectrum in patients with Alport syndrome-diffuse leiomyomatosis complex. Hum Mol Genet. 2015;24(20):5748-5758.

other2015
4

Kruegel J, Rubel D, Gross O. Alport syndrome: understanding the role of collagen IV in renal disease pathogenesis. Nat Rev Nephrol. 2013;9(4):200-210.

review2013

Medication Comparisons

Compare medications used to treat X Linked Diffuse Leiomyomatosis Alport Syndrome C1839884. 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