Naegeli-Franceschetti-Jadassohn Syndrome: eMedicine Dermatology
Links shared publicly online about this topic.
- 1,223total visits
Naegeli-Franceschetti-Jadassohn Syndrome: eMedicine Dermatology
View full resource at emedicine.medscape.com
Tags: Dermatology, Skin, Nails, Gland, Dental, Teeth, Disease and Condition
Most Recently Shared on May 5, 2010 at 2:37 pm By:
Naegeli-Franceschetti-Jadassohn Syndrome updated for 2010: http://bit.ly/cauFOe
Also Shared By:
Infantile Hemangioma: eMedicine Dermatology
emedicine.medscape.com — “Overview: Infantile hemangiomas are benign vascular neoplasms that have a characteristic clinical course marked by early proliferation and followed by spontaneous involution. During the proliferative phase in the neonatal period or early infancy, a rapidly dividing endothelial ...” View full resource at emedicine.medscape.com
Most Recently Shared on June 10, 2010 at 2:25 pm By:
Infantile hemangioma treatment with propranolol: http://bit.ly/aLZdhk
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
Chickenpox: eMedicine Dermatology
emedicine.medscape.com — “Overview: The varicella-zoster virus (VZV) is the etiologic agent of the clinical syndrome of chickenpox (varicella). Zoster, a different clinical entity, is caused by reactivation of VZV after primary infection. VZV is a double-stranded DNA virus included ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 23, 2010 at 3:31 am By:
The varicella-zoster virus (VZV) is the etiologic agent of the clinical syndrome of chickenpox (varicella). Learn more. http://bit.ly/bYWMmm
Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: eMedicine Dermatology
emedicine.medscape.com — “Overview: Toxic epidermal necrolysis (TEN) is an acute dermatologic disease, the presentation of which may constitute a true emergency. The disorder is characterized by widespread erythematous macules and targetoid lesions; full-thickness epidermal necrosis, at least focally; and ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 22, 2010 at 4:21 pm By:
Both Stevens-Johnson syndrome and toxic epidermal necrolysis can both constitute emergencies. See what else they share.http://bit.ly/bZQppO
Acute Febrile Neutrophilic Dermatosis: eMedicine Dermatology
emedicine.medscape.com — “Overview: Acute febrile neutrophilic dermatosis, also termed Sweet syndrome, is a reactive process characterized by the abrupt onset of tender, red-to-purple papules, and nodules that coalesce to form plaques. The plaques usually occur on the upper extremities, ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 22, 2010 at 4:08 pm By:
Acute febrile neutrophilic dermatosis (Sweet syndrome) results in the sudden appearance of tender lumps on the skin.http://bit.ly/95PYx0
Brachioradial Pruritus: eMedicine Dermatology
emedicine.medscape.com — “Overview: INTRODUCTION Brachioradial pruritus is a neurogenic itch syndrome of the upper extremities. It is typically localized to the skin on the dorsolateral forearm overlying the proximal head of the brachioradialis muscle, but involvement of the upper arms ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 22, 2010 at 3:52 pm By:
Brachioradial pruritus is a skin condition that is known to cause intense itching on the arms. http://bit.ly/be2j9T
Wells Syndrome (Eosinophilic Cellulitis): eMedicine Dermatology
emedicine.medscape.com — “Overview: In 1971, George Wells first described this syndrome as a recurrent granulomatous dermatitis with eosinophilia.1 Wells and Smith renamed it eosinophilic cellulitis in 1979.2Eosinophilic cellulitis (Wells syndrome) is an uncommon condition of unknown etiology. ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 22, 2010 at 3:54 am By:
Wells syndrome (eosinophilic cellulitis) is a condition of unknown cause. Learn the symptoms. http://bit.ly/dimmIG
Favre-Racouchot Syndrome (Nodular Elastosis With Cysts and Comedones): eMedicine Dermatology
emedicine.medscape.com — “Overview: Favre-Racouchot syndrome is a disorder consisting of multiple open and closed comedones in the presence of actinically damaged skin. The disease was originally described in 1932 by Favre1 and reviewed in detail by Favre and ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:50 pm By:
Favre-Racouchot syndrome is a skin condition involving blackheads or whiteheads and skin thickening. Learn causes. http://bit.ly/dp9xjg
Werner Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: Otto Werner originally defined Werner syndrome (WS) in 1904 on the basis of sclerodermalike, thin, tight skin and bilateral cataracts. WS is also known as progeria adultorum, progeria of the adult, and pangeria. WS is the ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:47 pm By:
Warner syndrome is the most common of all premature aging disorders. Learn the causes and symptoms. http://bit.ly/aJbyzs
Winchester Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: Winchester syndrome (WS) is a syndrome of pathologic changes consisting of dwarfism (resulting from disturbances of the skeletal-articular system), corneal opacities, coarsening of facial features, leathery skin, and hypertrichosis. In 1969, Winchester et al first described ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:43 pm By:
Winchester syndrome (WS) is a syndrome of pathologic changes consisting of dwarfism, eye problems, and skin changes. http://bit.ly/cnJfVE
Wiskott-Aldrich Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: Wiskott-Aldrich syndrome (WAS) is an X-linked recessive disorder originally described as a clinical triad of thrombocytopenia, eczema (atopiclike dermatitis), and recurrent pyogenic infections. Only 27% of patients have the classic triad, 20% of patients have hematologic ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:40 pm By:
Wiskott-Aldrich syndrome is a rare condition that affects blood cells and immune system cells. Learn more. http://bit.ly/dxaGuq
Refsum Disease: eMedicine Dermatology
emedicine.medscape.com — “Overview: Refsum disease (RD) is a neurocutaneous syndrome that is characterized biochemically by the accumulation of phytanic acid in plasma and tissues. Patients with Refsum disease are unable to degrade phytanic acid because of a deficient activity ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 11:25 pm By:
Refsum disease is a genetic disorder in which problems arise maintain nerve coverings. Learn more about symptoms. http://bit.ly/d0d0OJ
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
Advertisement




Susan Scroggins
@SusanS_Health
Wells syndrome (eosinophilic cellulitis) is a condition of unknown cause. Learn the symptoms. http://bit.ly/dimmIG
1 year ago...