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Poikiloderma vasculare atrophicans (PVA), is a cutaneous condition (skin disease) characterized by hypo- or hyperpigmentation (diminished or heightened skin pigmentation, respectively), telangiectasia and skin atrophy. [3] [4] [5] Other names for the condition include prereticulotic poikiloderma and atrophic parapsoriasis. [6]
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.
Poikiloderma vasculare atrophicans, a skin disease; Polyvinyl acetate, an adhesive used for porous materials like wood, paper, and cloth; Polyvinyl alcohol, a water-soluble synthetic polymer; Population viability analysis, a risk-assessment method used in conservation biology; Positive vorticity advection in meteorology
Hereditary sclerosing poikiloderma Keratosis pilaris; Heterochromia iridum; Holocarboxylase synthetase deficiency; Hypohidrotic ectodermal dysplasia (anhidrotic ectodermal dysplasia, Christ–Siemens–Touraine syndrome) Hypotrichosis–acro-osteolysis–onychogryphosis–palmoplantar keratoderma–periodontitis syndrome
Hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis is a rare genetic syndrome characterised by poikiloderma, tendon contractures and progressive pulmonary fibrosis. [1] It is also known as POIKTMP syndrome.
Large plaque parapsoriasis are skin lesions that may be included in the modern scheme of cutaneous conditions described as parapsoriasis. [2] These lesions, called plaques, may be irregularly round-shaped to oval and are 10 cm (4 in) or larger in diameter. [2]
Kindler syndrome (also known as "bullous acrokeratotic poikiloderma of Kindler and Weary" [1]) is a rare congenital disease of the skin caused by a mutation in the KIND1 gene. Symptoms and signs [ edit ]
Acrokeratotic poikiloderma; Adams–Oliver syndrome; Adult progeria; AEC syndrome; Albright's disease; Albright's hereditary osteodystrophy; Alopecia congenita with keratosis palmoplantaris; Alpha-N-acetylgalactosaminidase deficiency; Angelman syndrome; Anhidrotic ectodermal dysplasia; Ankyloblepharon filiforme adnatum–ectodermal dysplasia ...