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AJ Institute of Medical Science
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
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- Title:
- Congenital Rubella
- 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.
- Keyword:
- mental retardation, deafness, congenital, eye abnormalities, New born, Viral infection, RNA Virus Infections
- Subject:
- Togaviridae Infections, Rubella Syndrome, Congenital, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Congenital Abnormalities, Virus Diseases, Abnormalities, Multiple
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 2088
- Title:
- Congenital Rubella
- 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.
- Keyword:
- New born, Viral infection, mental retardation, RNA Virus Infections, eye abnormalities, deafness, congenital
- Subject:
- Virus Diseases, Togaviridae Infections, Abnormalities, Multiple, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Congenital Abnormalities, Rubella Syndrome, Congenital
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 2087
- Title:
- Congenital Rubella
- 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.
- Keyword:
- RNA Virus Infections, deafness, mental retardation, Viral infection, New born, eye abnormalities, congenital
- Subject:
- Abnormalities, Multiple, Togaviridae Infections, Congenital Abnormalities, Virus Diseases, Rubella Syndrome, Congenital, Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 2086
- Title:
- Tuberous Xanthoma
- Description:
- Tuberous xanthoma over thigh Xanthoma tuberosum is a yellow or orange flat or elevated round papule occurring in clusters on the skin of joints, especially the elbows and knees, usually in people who have a hereditary lipid storage disease such as hyperlipoproteinemia. The xanthomatous papules also may be associated with biliary cirrhosis and myxedema. Also called tuberous xanthoma, xanthoma tuberosum multiplex.
- Keyword:
- hypercholesterolemia, Congenital, Hyperlipoproteinemia Type II, familial, Papule, Hereditary, hpercholesterolemic xanthomatosis
- Subject:
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 2050
- Title:
- Congenital Rubella
- 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.
- Keyword:
- eye abnormalities, Viral infection, RNA Virus Infections, deafness, congenital, New born, mental retardation
- Subject:
- Rubella Syndrome, Congenital, Togaviridae Infections, Congenital Abnormalities, Virus Diseases, Abnormalities, Multiple, Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 2085
- Title:
- Herpes Genitalis
- Description:
- Herpes genitalis in prepubertal child
- Keyword:
- virus, Sexually transmitted disease, genitals, sex organs, Hemophilia A
- Subject:
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 2091
- Title:
- Epidermolysis Bullosa Congenita
- 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.
- Keyword:
- Skin Diseases, Vesiculobullous, nail changes, severe scarring, atrophy of blistered areas, Congenital disease
- Subject:
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin and Connective Tissue Diseases, Skin Abnormalities, Skin Diseases, Genetic, Epidermolysis Bullosa, Collagen Diseases, Congenital Abnormalities, Skin Diseases, Connective Tissue Diseases, Genetic Diseases, Inborn, Epidermolysis Bullosa Dystrophica
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 1918
- Title:
- Epidermolysis Bullosa Congenita
- 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.
- Keyword:
- severe scarring, atrophy of blistered areas, Skin Diseases, Vesiculobullous, nail changes, Congenital disease
- Subject:
- Epidermolysis Bullosa Dystrophica, Congenital Abnormalities, Genetic Diseases, Inborn, Collagen Diseases, Skin Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin Diseases, Skin Diseases, Genetic, Epidermolysis Bullosa, Connective Tissue Diseases, Skin and Connective Tissue Diseases
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 1917
- Title:
- Epidermolysis Bullosa Congenita
- 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.
- Keyword:
- severe scarring, Congenital disease, nail changes, Skin Diseases, Vesiculobullous, atrophy of blistered areas
- Subject:
- Connective Tissue Diseases, Collagen Diseases, Skin Abnormalities, Skin Diseases, Genetic Diseases, Inborn, Skin Diseases, Genetic, Epidermolysis Bullosa Dystrophica, Skin and Connective Tissue Diseases, Epidermolysis Bullosa, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 1920
- Title:
- Epidermolysis Bullosa Congenita
- 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.
- Keyword:
- Skin Diseases, Vesiculobullous, nail changes, severe scarring, Congenital disease, atrophy of blistered areas
- Subject:
- Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin Diseases, Skin Abnormalities, Connective Tissue Diseases, Epidermolysis Bullosa, Congenital Abnormalities, Skin and Connective Tissue Diseases, Epidermolysis Bullosa Dystrophica, Collagen Diseases, Skin Diseases, Genetic
- Creator:
- Dr. P.N. Girish, MBBS, MD, DDV, DNB AJ Institute of Medical Science
- Publisher:
- AJ Institute of Medical Science
- Language:
- English
- Copyright Holder:
- AJ Institute of Medical Science
- Rights:
- http://www.i-human.com/service-agreement-print
- Resource Type:
- Photo
- Identifier:
- 1922