Familiar palmoplantar keratoderma, flaccid blisters, and widespread scaling. [PDF]
JAAD Case Rep, 2018 Oliveira LM +5 more
europepmc +1 more source
Concurrent superficial epidermolytic ichthyosis and generalized pustular psoriasis - Report of a case, review of the literature, and a proposed pathophysiologic link. [PDF]
JAAD Case RepHan JY +4 more
europepmc +1 more source
First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses. [PDF]
Int J Mol Sci, 2020 Diociaiuti A +9 more
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Hereditary Palmoplantar Keratoderma: A Practical Approach to the Diagnosis. [PDF]
Indian Dermatol Online J, 2019 Dev T, Mahajan VK, Sethuraman G.
europepmc +1 more source
Inherited epidermolysis bullosa: update on the clinical and genetic aspects. [PDF]
An Bras Dermatol, 2020 Mariath LM +3 more
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Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues [PDF]
, 2007 Irvine, Alan D, McLean, WH Irwin
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Harlequin ichthyosis and ABCA12
, 2012 MD(Res)Harlequin ichthyosis (HI), a rare severe form of congenital ichthyosis is caused by recessive mutations in the ABCA12 gene. At birth, affected neonates have widespread, grossly thickened skin, separated by deep red fissures, bilateral ectropion ...
Rajpopat, Shefali
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Epidermolytic hyperkeratosis: clinical update. [PDF]
Clin Cosmet Investig Dermatol, 2019 Peter Rout D, Nair A, Gupta A, Kumar P.
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A case of a patient with severe epidermolysis bullosa surviving to adulthood. [PDF]
Int J Gen Med, 2018 Hubail AR +3 more
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