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Arvelig palmoplantar keratodermi

Forfatter(e)
Shailajah Kamaleswaran1, Lilian Bomme Ousager2, Rasmus Overgaard Bach3 & Anette Bygum3 1) Klinisk Genetisk Afdeling, Aalborg Universitetshospital 2) Klinisk Genetisk Afdeling, Odense Universitetshospital 3) Hudafdeling I og Allergicentret, Odense Universitetshospital Ugeskr Læger 2014;176:V05130280
Reference: 
Ugeskr Læger 2015;177:V05130280
Blad nummer: 
Sidetal: 
457-461
Hereditary palmoplantar keratoderma – a focus on clinical and molecular genetic aspects
Hereditary palmoplantar keratoderma comprises a heterogenous group of genodermatoses. The clinical spectrum of palmoplantar keratoderma can range from pure skin thickening, restricted to palmoplantar skin to complex conditions with dental anomalies, eye symptoms, deafness, cardiac disease and cancer. The classification of hereditary palmoplantar keratoderma has been complicated. In recent years the molecular genetic background has been clarified for an increasing number of palmoplantar keratodermas, which makes it possible to make a more accurate diagnosis.
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