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  1. Epidermolysis Bullosa Congenita

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    Description: Epidermolysis bullosa congenita - multiple blisters over the feet Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in collagen type VII, a major component fibrils of basement membrane and epidermis.
    Keywords: severe scarring, atrophy of blistered areas, Skin Diseases, Vesiculobullous, nail changes, Congenital disease

  2. Epidermolysis Bullosa Congenita

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    Description: Epidermolysis bullosa congenita - erosions with post-inflammatory dyspigmentation over the abdomen Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in collagen type VII, a major component fibrils of basement membrane and epidermis.
    Keywords: severe scarring, Congenital disease, nail changes, Skin Diseases, Vesiculobullous, atrophy of blistered areas

  3. Epidermolysis Bullosa Congenita

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    Description: Epidermolysis bullosa congenita - multiple bullae, crusted erosions over the face Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in collagen type VII, a major component fibrils of basement membrane and epidermis.
    Keywords: Skin Diseases, Vesiculobullous, nail changes, severe scarring, Congenital disease, atrophy of blistered areas

  4. Epidermolysis Bullosa Congenita

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    Description: Epidermolysis bullosa congenita - multiple blisters over the weight-bearing areas Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in collagen type VII, a major component fibrils of basement membrane and epidermis.
    Keywords: severe scarring, Congenital disease, Skin Diseases, Vesiculobullous, nail changes, atrophy of blistered areas

  5. Hand Tophi, Gout

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    Description: Gout - hand tophi
    Keywords: joint, arthritis, Inflammation

  6. Finger Tophi, Gout

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    Description: Gout - finger tophi
    Keywords: Inflammation, arthritis, joint

  7. Ear Tophi, Gout

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    Description: Gout - ear tophi
    Keywords: Inflammation, arthritis, joint

  8. Gout Crystals

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    Description: Gout crystals
    Keywords: Inflammation, arthritis, joint

  9. Toe Tophi, Gout

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    Description: Toe tophi Gout
    Keywords: Inflammation, arthritis, joint

  10. Ultrasound (abdomen), Wilms Tumor

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    Description: US Abdomen Complete, 9 yo M, 1a= AP
    Keywords: Wilms Tumor 1, Wilms Tumor, Diagnosis, Echography, Echotomography, Computer, Ultrasound Imaging, Tomography, Ultrasonic, Neoplasms, Diagnosis, Ultrasonic, Ultrasonic Tomography, Nephroblastoma, Echotomography, Wilms' Tumor, Ultrasonic Imaging, Ultrasonic Diagnosis, Computer Echotomography, Neoplasms by Histologic Type, Sonography, Medical, Bilateral Wilms Tumor