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Abstract

The ichthyoses represent a large heterogeneous group of Mendelian disorders of keratinization (cornification), clinically characterized by the presence of scales on the skin. They may manifest at birth or later on, and they could be isolated or associated with extracutaneous anomalies. The choice of treatment depends on the type of ichthyoses, age of the patient, the involved areas, and the extent of the disease.

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Abbreviations

ARCI:

Autosomal Recessive Congenital Ichthyosis

TGM1:

Transglutaminase 1 gene

ABCA12:

gene ATP-binding cassette, sub-family A (ABC), member 12

ALOXE3:

gene arachidonatelipoxygenase 3

ALOX12B:

gene arachidonate 12-lipoxygenase, 12R type

FLJ39501:

gene

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Correspondence to Mauro Paradisi .

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Paradisi, M., El Hachem, M., Diociaiuti, A., Giannetti, A. (2015). Ichthyoses. In: Katsambas, A.D., Lotti, T.M., Dessinioti, C., D’Erme, A.M. (eds) European Handbook of Dermatological Treatments. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-45139-7_44

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  • DOI: https://doi.org/10.1007/978-3-662-45139-7_44

  • Publisher Name: Springer, Berlin, Heidelberg

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