Epidermolysis bullosa
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Summary of Epidermolysis bullosa
Epidermolysis bullosa encompasses a clinically and genetically heterogeneous group of rare inherited disorders characterized by marked mechanical fragility of epithelial tissues with blistering and erosions following minor trauma.
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Integumentary system
Pathology
Pigmented skin disorders
Acneiform skin disorders
Papulosquamous and inflammatory skin disorders
Keratotic skin disorders
Vesiculobullous skin disorders
Desquamating skin disorders
Skin integrity disorders
Skin infections
Cellulitis
Erysipelas
Impetigo
Necrotizing fasciitis
Human papillomavirus
Varicella zoster virus
Poxvirus (Smallpox and Molluscum contagiosum)
Coxsackievirus
Herpes simplex virus
Candida
Malassezia (Tinea versicolor and Seborrhoeic dermatitis)
Pediculus humanus and Phthirus pubis (Lice)
Sarcoptes scabiei (Scabies)
Human herpesvirus 6 (Roseola)
Parvovirus B19
Varicella zoster virus
Measles virus
Rubella virus
Skin neoplasms
Hair and nail disorders
Integumentary system pathology review
AssessmentsEpidermolysis bullosa
Epidermolysis bullosa
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Questions
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Flashcards
Epidermolysis bullosa
8 flashcards
Questions
USMLE® Step 1 style questions USMLE
1 questions
Preview
A patient presents to the clinic for the first time. She informs the physician that the skin on her hands and feet has always been very fragile and bruises easily with minor injury or friction. The blisters usually heal and do not leave a scar. The physician diagnoses the patient with epidermolysis bullosa simplex. Which statement below most accurately describes the protein that is altered in this disease?
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Epidermolysis bullosa exam links
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