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A 20-year-old female patient with the typical signs of Wissler's subsepsis allergica (Wissler-Fanconi syndrome) is described. This rare disease is characterized by four typical symptoms: polymorphous exanthemas, recurrent high fever, leucocytosis and arthralgia. In the early stages it is difficult to differentiate from septicaemia.

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[Subsepsis allergica in a patient with type I polyglandular autoimmune syndrome].

Monatsschr Kinderheilkd

September 1990

Kinderklinik des St.-Marien- und St.-Annastifts-Krankenhauses, Ludwigshafen.

A 10.6 year old Turkish girl developed + the signs of a polyglandular autoimmune syndrome (PGA) type I since her first year of age. Apart from the endocrine and non-endocrine symptoms of PGA, she suffered from an acute state of illness with therapy-resistant fever and multiform exanthemas in the early course of disease.

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