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Granulomatous Disease Chronic Autosomal Recessive 5 C5394542

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

An inherited immune disorder where white blood cells cannot kill certain bacteria and fungi, leading to recurrent infections. Lifelong management with preventive antibiotics is typically needed.

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

Key facts at a glance

ICD-10
D89.9
ICD-11
3A00.0
Body system
immunologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Generalized symptoms

(immunologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Recurrent pneumonia

(respiratory)

Skin abscess

(integumentary)

Hepatic abscess

(hepatobiliary)

Osteomyelitis

(musculoskeletal)

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

Prophylactic Antimicrobial Therapy

Continuous preventive antibiotics such as trimethoprim-sulfamethoxazole or itraconazole to reduce frequency and severity of bacterial and fungal infections.

medication
2

Targeted drug therapy with dose adjustment

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

medication
3

Immunoglobulin Replacement Therapy

Regular intravenous or subcutaneous immunoglobulin infusions to provide passive immunity against common pathogens that patients cannot effectively combat.

medication

Additional treatment options

Infection Surveillance Program

Regular clinical assessments and laboratory monitoring for early detection of infections and inflammatory complications including granuloma formation.

monitoring

Granuloma Management Procedures

Surgical intervention for symptomatic granulomas causing obstruction or tissue damage, including drainage, resection, or corrective procedures.

surgical

Infection Prevention Practices

Rigorous hand hygiene, food safety measures, respiratory precautions, and avoidance of environmental sources of infection to minimize exposure risks.

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 Granulomatous Disease Chronic Autosomal Recessive 5 C5394542?

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

general

Medication Comparisons

Compare medications used to treat Granulomatous Disease Chronic Autosomal Recessive 5 C5394542. 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