Aktinische Prurigo

Worret, W.-I.; Vocks, E.; Frías, Gabriela; Burgdorf, Walter H. C.; Lane, Peter R.

doi:10.1007/s001050051156

Cited by 10 publications

(2 citation statements)

References 21 publications

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“…In jüngster Zeit wurden jedoch auch vermehrt Familien mit AP beschrieben, die europäischer Abstammung sind, vornehmlich in Finnland, England, Deutschland und Österreich[24,55]. Diese neueren Erkenntnisse könnten Anlass sein, die traditionelle Klassifikation dieser Erkrankung zu überdenken und zu revidieren.durchzuführen.…”

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Hereditäre Photodermatosen

et al. 2006

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Hereditary photodermatoses are characterized by an increased photosensitivity caused by an inherited single gene defect. With few exceptions, they manifest in early childhood, reveal heterogeneous clinical symptoms, and are difficult to treat. Although these diseases are rare, it is very important to make an accurate diagnosis on the basis of clinical symptoms, specific diagnostic tests, and direct DNA analysis. We review the spectrum of inherited photodermatoses, including porphyria cutanea tarda, erythropoietic protoporphyria, actinic prurigo, Kindler syndrome, and disorders associated with a defect in DNA repair, including xeroderma pigmentosum, trichothiodystrophy, Cockayne syndrome, and Bloom syndrome. Early diagnosis may prevent complications associated with prolonged unprotected exposure to sunlight and makes it possible to offer genetic counseling and, when indicated, prenatal diagnosis to families at risk for these rare heritable disorders.

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Hereditäre Photodermatosen

et al. 2006

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“…Eine familiäre Variante kommt bei Indianern in Nord-und Lateinamerika vor. Sie wird dort als hereditäre polymorphe Lichtdermatose oder familiäre aktinische Prurigo bezeichnet(12,23,39,41). Stufentherapie der polymorphen Lichtdermatose.…”

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