People with varying manifestations of poikiloderma
Specialty
Dermatology
Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy.
Poikiloderma of Civatte is most frequently seen on the chest or the neck, characterized by red colored pigment on the skin that is commonly associated with sun damage.[1]
^Raulin, Christian; Karsai, Syrus (2011). Laser and IPL Technology in Dermatology and Aesthetic Medicine. Springer Science & Business Media. p. 236. ISBN 9783642034381. Retrieved 7 March 2018.
Poikiloderma is a skin condition that consists of areas of hypopigmentation, hyperpigmentation, telangiectasias and atrophy. Poikiloderma of Civatte is...
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary") is a rare congenital disease of the skin caused by a mutation...
Poikiloderma vasculare atrophicans (PVA), is a cutaneous condition (skin disease) characterized by hypo- or hyperpigmentation (diminished or heightened...
Poikiloderma of Civatte is a cutaneous condition and refers to reticulated red to red-brown skin patches with telangiectasias. It is identifiable as a...
Hereditary sclerosing poikiloderma is an autosomal dominant conditions with skin changes consisting of generalized poikiloderma appearing in childhood...
poikiloderma, bullous acrokeratotic poikiloderma of Kindler and Weary, congenital poikiloderma with blisters and keratoses, congenital poikiloderma with...
Side effects may be mild such as itchiness, folliculitis, sunburn, poikiloderma, and a theoretical risk of nonmelanoma cancer or melanoma has been suggested...
right third intercostal nerve through its anterior cutaneous branch. Poikiloderma of Civatte, a condition of dilated blood vessels and red to red-brown...
Incontinentia pigmenti (IP) is a rare X-linked dominant genetic disorder that affects the skin, hair, teeth, nails and central nervous system. It is named...
scapular anomalies Pierre Robin syndrome-faciodigital anomaly syndrome Poikiloderma with neutropenia Polymicrogyria with or without vascular-type Ehlers-Danlos...
syndrome, also known as poikiloderma congenitale, is characterized by premature aging, skin and skeletal abnormalities, rash, poikiloderma, juvenile cataracts...
Hereditary spastic paraplegia (HSP) is a group of inherited diseases whose main feature is a progressive gait disorder. The disease presents with progressive...
tissue, usually occurs within the area of these plaques. Parapsoriasis Poikiloderma vasculare atrophicans List of cutaneous conditions Lambert WC, Everett...