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  1. Congenital Rubella

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    Description: Congenital rubella - multiple dusky red purpuric patches and plaques over the body Congenital rubella syndrome (CRS) can occur in a developing fetus of a pregnant woman who has contracted rubella during her first trimester. If infection occurs 0–28 days before conception, there is a 43% chance the infant will be affected. If the infection occurs 0–12 weeks after conception, there is a 51% chance the infant will be affected. If the infection occurs 13–26 weeks after conception there is a 23% chance the infant will be affected by the disease. Infants are not generally affected if rubella is contracted during the third trimester, or 26–40 weeks after conception. Problems rarely occur when rubella is contracted by the mother after 20 weeks of gestation and continues to disseminate the virus after birth.
    Keywords: mental retardation, deafness, congenital, eye abnormalities, New born, Viral infection, RNA Virus Infections

  2. Congenital Rubella

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    Description: Congenital rubella lesions over abdomen/trunk Congenital rubella syndrome (CRS) can occur in a developing fetus of a pregnant woman who has contracted rubella during her first trimester. If infection occurs 0–28 days before conception, there is a 43% chance the infant will be affected. If the infection occurs 0–12 weeks after conception, there is a 51% chance the infant will be affected. If the infection occurs 13–26 weeks after conception there is a 23% chance the infant will be affected by the disease. Infants are not generally affected if rubella is contracted during the third trimester, or 26–40 weeks after conception. Problems rarely occur when rubella is contracted by the mother after 20 weeks of gestation and continues to disseminate the virus after birth.
    Keywords: New born, Viral infection, mental retardation, RNA Virus Infections, eye abnormalities, deafness, congenital

  3. Congenital Rubella

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    Description: Congenital rubella - lesions over feet Congenital rubella syndrome (CRS) can occur in a developing fetus of a pregnant woman who has contracted rubella during her first trimester. If infection occurs 0–28 days before conception, there is a 43% chance the infant will be affected. If the infection occurs 0–12 weeks after conception, there is a 51% chance the infant will be affected. If the infection occurs 13–26 weeks after conception there is a 23% chance the infant will be affected by the disease. Infants are not generally affected if rubella is contracted during the third trimester, or 26–40 weeks after conception. Problems rarely occur when rubella is contracted by the mother after 20 weeks of gestation and continues to disseminate the virus after birth.
    Keywords: RNA Virus Infections, deafness, mental retardation, Viral infection, New born, eye abnormalities, congenital

  4. 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

  5. Congenital Rubella

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    Description: Congenital rubella - blueberry muffin lesions over face Congenital rubella syndrome (CRS) can occur in a developing fetus of a pregnant woman who has contracted rubella during her first trimester. If infection occurs 0–28 days before conception, there is a 43% chance the infant will be affected. If the infection occurs 0–12 weeks after conception, there is a 51% chance the infant will be affected. If the infection occurs 13–26 weeks after conception there is a 23% chance the infant will be affected by the disease. Infants are not generally affected if rubella is contracted during the third trimester, or 26–40 weeks after conception. Problems rarely occur when rubella is contracted by the mother after 20 weeks of gestation and continues to disseminate the virus after birth.
    Keywords: eye abnormalities, Viral infection, RNA Virus Infections, deafness, congenital, New born, mental retardation

  6. Port-Wine Stain

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    Description: Port-wine stain (PWS) with angiomatous nodule Port-wine stain is a purplish area of the skin, usually on the head and neck, appearing at birth and caused by an overgrowth of the cutaneous capillaries. Also called nevus flammeus, port-wine mark.
    Keywords: erythema, Port-Wine Stain, port wine stain, purple, Skin

  7. 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

  8. 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

  9. 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

  10. 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