Junctional Epidermolysis Bullosa Non Herlitz Type C0268374
A genetic skin blistering condition causing fragile skin that blisters easily with minor trauma. Generally less severe than other junctional types. Treatment includes wound care and monitoring.
Key facts at a glance
- ICD-10
- Q84.9
- ICD-11
- LA00.0
- Body system
- dermatologic
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Generalized symptoms
(dermatologic)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
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
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Gentle Skin Care Protocol
Daily cleansing with mild, fragrance-free soaps and regular application of emollients to maintain skin hydration and reduce mechanical trauma.
Protective Bandaging Techniques
Use of soft, non-adhesive dressings with protective padding over friction-prone areas to minimize blister formation during daily activities.
When to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Junctional Epidermolysis Bullosa Non Herlitz Type C0268374?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy