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You searched for: Language English Remove constraint Language: English Subject Genetic Diseases, Inborn Remove constraint Subject: Genetic Diseases, Inborn
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  1. Steatocystoma Multiplex

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    Description: Steatocystoma multiplex - multiple yellowish papulonodules over scrotum A skin disorder marked by the development of many sebaceous cysts.
    Keywords: cysts on skin, Ectodermal Diseases, lobule, Sebaceous cysts

  2. Herpes Genitalis

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    Description: Herpes genitalis in prepubertal child
    Keywords: virus, Sexually transmitted disease, genitals, sex organs, Hemophilia A

  3. Epidermolysis Bullosa Congenita

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    Description: Epidermolysis bullosa congenita - bullae over the pressure points 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, atrophy of blistered areas, Congenital disease

  4. 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

  5. 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

  6. 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

  7. 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

  8. Hand Tophi, Gout

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

  9. Finger Tophi, Gout

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

  10. Ear Tophi, Gout

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