Congenital Nevi: eMedicine Dermatology
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Congenital Nevi: eMedicine Dermatology
View full resource at emedicine.medscape.com
Tags: Dermatology, Skin, Childbirth
Most Recently Shared on April 21, 2010 at 3:38 am By:
A congenital nevi is moles that are present at or develops shortly after birth. http://bit.ly/dC8Ed5
Melanocytic Nevi - Congenital Nevi - Skin Conditions Explained - Anthony J. Perri, M.D.
perridermatology.com — “Melanocytic Nevi - Congenital Nevi - Skin Conditions Explained - Anthony J. Perri, M.D.” View full resource at perridermatology.com
Most Recently Shared on September 6, 2011 at 1:20 pm By:
Congenital Nevi are melanocytic nevi that are present at birth, thus many patients refer to them as "birthmarks." http://ht.ly/6m1a7
Giant Congenital Melanocytic Nevi May Signal Melanoma in Kids : Skin & Allergy News
skinandallergynews.com — “Skin & Allergy News Digital Network is the online destination and multimedia properties of Skin & Allergy News, the independent news publication for the dermatology community. Our breaking news covers all areas of medical dermatology, dermatologic surgery, and aesthetic dermatology. We also provide the news by specialty interest: acne and rosacea, atopic dermatitis and eczema, cutaneous oncology, hair and nails, infectious diseases, pediatric dermatology, psoriasis and rheumatologic disorders, s” View full resource at skinandallergynews.com
Most Recently Shared on July 28, 2011 at 7:01 pm By:
"The child who is born with multiple small congenital nevi [a birthmark or mole]... has a risk factor": http://bit.ly/oEVzjX
Giant Congenital Melanocytic Nevi May Signal Melanoma in Kids : Skin & Allergy News
skinandallergynews.com — “Skin & Allergy News Digital Network is the online destination and multimedia properties of Skin & Allergy News, the independent news publication for the dermatology community. Our breaking news covers all areas of medical dermatology, dermatologic surgery, and aesthetic dermatology. We also provide the news by specialty interest: acne and rosacea, atopic dermatitis and eczema, cutaneous oncology, hair and nails, infectious diseases, pediatric dermatology, psoriasis and rheumatologic disorders, s” View full resource at skinandallergynews.com
Most Recently Shared on July 27, 2011 at 9:50 pm By:
Giant congenital melanocytic nevi in kids assoc w increased melanoma risk. Condition is rare: 1 in 100,000 births http://bit.ly/q6OeE5
Giant Congenital Melanocytic Nevi May Signal Melanoma in Kids : Skin & Allergy News
skinandallergynews.com — “Skin & Allergy News Digital Network is the online destination and multimedia properties of Skin & Allergy News, the independent news publication for the dermatology community. Our breaking news covers all areas of medical dermatology, dermatologic surgery, and aesthetic dermatology. We also provide the news by specialty interest: acne and rosacea, atopic dermatitis and eczema, cutaneous oncology, hair and nails, infectious diseases, pediatric dermatology, psoriasis and rheumatologic disorders, s” View full resource at skinandallergynews.com
Most Recently Shared on July 27, 2011 at 3:54 pm By:
Giant Congenital Melanocytic Nevi May Signal Melanoma in Kids http://tinyurl.com/3pgs9kx
Congenital Self-Healing Reticulohistiocytosis: eMedicine Dermatology
emedicine.medscape.com — “Overview: INTRODUCTION Langerhans cell histiocytosis (LCH), once described as histiocytosis X, is a clonal proliferative disorder of Langerhans cells that stain immunohistochemically with S-100 and CD-1a and demonstrate cytoplasmic Birbeck granules under electron microscopy.1 Four variants of ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 1, 2010 at 7:38 pm By:
Extensive erosive lesions in congenital self-healing reticulohistiocytosis: http://bit.ly/9s8fuk
Rubella: eMedicine Dermatology
emedicine.medscape.com — “Overview: Rubella is usually a mild viral illness involving the skin, the lymph nodes, and, less commonly, the joints. The most important complication of rubella is congenital rubella syndrome (CRS). Pathophysiology Rubella is an RNA virus classified ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 23, 2010 at 3:46 am By:
Rubella is usually a mild viral illness involving the skin, the lymph nodes, and, less commonly, the joints. Learn more.http://bit.ly/a4CX1g
Supernumerary Nipple: eMedicine Dermatology
emedicine.medscape.com — “Overview: Supernumerary nipples (SNs) are a common minor congenital malformation that consists of nipples and/or related tissue in addition to the 2 nipples normally appearing on the chest. SNs are located along the embryonic milk line. Ectopic ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:35 pm By:
Supernumerary nipples consists of nipples and/or related tissue in addition to the 2 nipples normally on the chest. http://bit.ly/djAAOm
Ulerythema: eMedicine Dermatology
emedicine.medscape.com — “Overview: Ulerythema ophryogenes, a rare cutaneous disorder, is characterized by inflammatory keratotic facial papules that may result in scars, atrophy, and alopecia. This disorder has been described in association with other congenital anomalies such as Noonan syndrome, ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:18 pm By:
Ulerythema ophryogenes is a relatively infrequent disorder that mainly affects children and young adults. Learn causes. http://bit.ly/aewdJc
Supernumerary Digit: eMedicine Dermatology
emedicine.medscape.com — “Overview: Polydactyly is the most common congenital digital anomaly of the hand and foot. It may appear in isolation or in association with other birth defects. Isolated polydactyly is often autosomal dominant or occasionally random, while syndromic ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:15 pm By:
Polydactyly is the most common congenital digital anomaly of the hand & foot.It may appear alone or with other defects.http://bit.ly/bttFma
Sjogren-Larsson Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: Sjogren-Larsson syndrome (SLS) is a rare autosomal recessive neurocutaneous disorder characterized by mental retardation, diplegia or tetraplegia, and congenital ichthyosis. The ichthyosis (usually evident at birth) may be seen in some patients after the first year ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:13 pm By:
Sjögren-Larsson syndrome is a genetic condition resulting in thickened, dry, rough skin, mental retardation & more. http://bit.ly/dC4eId
Niemann-Pick Disease: eMedicine Dermatology
emedicine.medscape.com — “Overview: Niemann-Pick disease (NPD) comprises an autosomal recessively inherited group of congenital lipidoses in which sphingolipids accumulate in cells, especially reticuloendothelial cells, throughout the body.The following 6 types of Niemann-Pick disease have been described:Type A - ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:05 pm By:
Niemann-Pick disease refers to a group of fatal inherited metabolic disorders. Learn more about Niemann-Pick disease. http://bit.ly/csRuX4
Preauricular Sinuses: eMedicine Dermatology
emedicine.medscape.com — “Overview: Preauricular sinuses are common congenital malformations first described by Heusinger in 1864. Preauricular sinuses are frequently noted on routine physical examination as small dells adjacent to the external ear, usually at the anterior margin of the ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 10:45 pm By:
Preauricular sinuses are frequently noted on routine physical examinations. What are they, and what is the cause? http://bit.ly/dwsAeT
Piebaldism: eMedicine Dermatology
emedicine.medscape.com — “Overview: Piebaldism is a rare autosomal dominant disorder of melanocyte development characterized by a congenital white forelock and multiple symmetrical hypopigmented or depigmented macules. This striking phenotype of depigmented patches of skin and hair has been observed ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 10:28 pm By:
Piebaldism is due to an absence of melanocytes in affected skin and hair follicles as a result of mutations. Learn more.http://bit.ly/9QAZlG
Kindler Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: First described in 1954 by Theresa Kindler, Kindler syndrome is a rare autosomal recessive genodermatosis characterized by congenital acral skin blistering, photosensitivity, progressive poikiloderma, and diffuse cutaneous atrophy. The syndrome is a combination of features of ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 9:01 pm By:
Kindler syndrome is a hereditary condition that results in blistering and photosensitivity during infancy. Learn more.http://bit.ly/9Zf8lp
Ichthyosis Fetalis: eMedicine Dermatology
emedicine.medscape.com — “Overview: Ichthyosis fetalis, also known as harlequin ichthyosis (HI), is the most severe form of congenital ichthyosis. It is characterized by a profound thickening of the keratin layer in fetal skin. The affected neonate is born with ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 8:51 pm By:
Ichthyosis fetalis, also known as harlequin ichthyosis (HI), is the most severe form of congenital ichthyosis. http://bit.ly/cycfCj
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