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Published byHannah Riley Modified over 9 years ago
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The Integumentary System Normal skin, Genetic Defects, and Scar Formation
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Cross section through human skin Keratin Stratified squamous epithelium Dense irregular connective tissue
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Cross section through human skin
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Pacinian corpuscle (note the onion-like appearance)
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Meissner corpuscles located in the dermis
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Melanin producing melanocytes
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Genetic Abnormalities Associated with Skin
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Epidermolysis Bullosa Fragile Skin, Blistering do to a defect in the adhesion molecules that keep the simple squamous epithelium together
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Ichthyosis – Scaly fish disorder Harlequin Type 1 ichthysos
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Neurofibromatosis – defect on Chromosome 1. Autoosmal dominant disorder
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Incontinentia Pigmenti X-linked disorder, often fatal in boys, causes hyperpigmentation of the skin, blistering, loss of motor function, delayed growth, mental impairment
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Albinism – A autosomal recessive genetic disorder in which the individual produces no melanin. Albinism occurs in all species and races
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Simplified cross section of a hair
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Scar Formation
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Normal healing, epithelial cells move to the areaLittle or no fibroblast activityNormal healing, epithelial cells move to the areaLittle or no fibroblast activity
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Mild hypertrophic scarring
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Mild keloid formation
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Keloid formation
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Cesarean section scars then and now
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Ritual scarification of the skin for religious or cultural reasons
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Scarification as body art / modification
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Diabetic ulceration of the foot, note the extensor tendons of the foot
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