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Other Genodermatoses

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Atlas of Skin Disorders

Abstract

Besides genodermatoses with presentation of keratoderma, other hereditary cutaneous diseases and syndromes considered in this chapter are incontinentia pigmenti, epidermolysis bullosa simplex, recessive dystrophic epidermolysis bullosa (generalized, severe), dystrophic epidermolysis bullosa pruriginosa, pretibial epidermolysis bullosa, Hailey-Hailey disease, ichthyosis bullosa of Siemens, bullous congenital ichthyosiform erythroderma, collodion baby, Rothmund-Thomson syndrome, Rapp-Hodgkin syndrome, focal dermal hypoplasia, aplasia cutis congenital, dyskeratosis congenita, rudimentary polydactyly, keratosis follicularis spinulosa decalvans, pachydermoperiostosis, xeroderma pigmentosum, cutis tricolor parvimaculata, congenital thymic dysplasia, pachyonychia congenita, Papillon-Lefèvre syndrome, Olmsted syndrome, nail-patella syndrome, Keratitis-ichthyosis-deafness syndrome, Netherton syndrome, Bloom’s syndrome, tricho-rhino-phalangeal syndrome, proteus syndrome, stiff skin syndrome, Rombo syndrome, prune-belly syndrome, infantile digital fibromatosis, and juvenile hyaline fibromatosis.

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Zhang, RZ. et al. (2018). Other Genodermatoses. In: Zhu, WY., Tan, C., Zhang, Rz. (eds) Atlas of Skin Disorders. Springer, Singapore. https://doi.org/10.1007/978-981-10-8037-1_26

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  • Online ISBN: 978-981-10-8037-1

  • eBook Packages: MedicineMedicine (R0)

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