Abstract
Genetically inherited dermatological conditions can be classified according to their clinical manifestations, irrespective of the mode of inheritance, which may be autosomal dominant, autosomal recessive or X-linked recessive. The hereditary cutaneous diseases comprise keratoses, bullous diseases, pigmentary anomalies, hyperplasias, naevi and naevoid tumours. The following genodermatoses are considered in this chapter:
-
Ichthyoses
-
Keratosis pilaris
-
Keratosis palmoplantaris
-
Mal de Meleda
-
Porokeratosis of Mibelli
-
Darier’s disease
-
Epidermolysis bullosa
-
Neurofibromatosis Recklinghausen
-
Adenoma sebaceum
-
Pseudoxanthoma elasticum
-
Trichoepithelioma
-
Xeroderma pigmentosum
-
Steatocystoma multiplex
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1994 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Schaller, K.F. (1994). Genodermatoses. In: Schaller, K.F. (eds) Colour Atlas of Tropical Dermatology and Venerology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-76200-0_14
Download citation
DOI: https://doi.org/10.1007/978-3-642-76200-0_14
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-76202-4
Online ISBN: 978-3-642-76200-0
eBook Packages: Springer Book Archive