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Epidermolytic Hyperkeratosis 2A
An epidermolytic hyperkeratosis that is characterized by blistering, keratoderma, and erythroderma that is caused by heterozygous or homozygous mutation in the keratin-10 gene on chromosome 17q21.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
An epidermolytic hyperkeratosis that is characterized by blistering, keratoderma, and erythroderma that is caused by heterozygous or homozygous mutation in the keratin-10 gene on chromosome 17q21.
Resources
Join the Epidermolytic Hyperkeratosis 2A community
Talk with people who understand, share what helps, and find support from others living with epidermolytic hyperkeratosis 2a. Private, moderated, and free.
Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.