A case of non-familial multiple digitate hyperkeratosis is reported. Digitate hyperkeratosis is a new, non-follicular disorder of keratinization and three different types have been distinguished in the literature: the familial type, with an autosomal dominant trait; the sporadic type; and the post-inflammatory type.
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http://dx.doi.org/10.1111/j.1365-2230.1993.tb02183.x | DOI Listing |
Int J Dermatol
October 2024
Department of Dermatology, Faculty of Medicine and Medical Sciences, Sana'a University, Sana'a, Yemen.
An Pediatr (Engl Ed)
May 2024
Departamento de Dermatología Pediátrica, Instituto Dermatológico de Jalisco "Dr. José Barba Rubio", Zapopan, Jalisco, México. Electronic address:
Am J Dermatopathol
July 2024
Department of Dermatology, Yale School of Medicine, New Haven, CT.
JAAD Case Rep
March 2024
Division of Dermatology, University of Kansas Medical Center, Kansas City, Kansas.
Pediatr Dermatol
May 2024
Division of Dermatology, Department of Pediatrics, CHU Sainte-Justine, Universite de Montreal, Montreal, Canada.
Infantile anogenital digitate keratoses (IADK) represent a distinct and under-recognized pediatric condition of the perianal area of infants, significantly more frequent in males than females. The average age of onset is 3.2 months, and it is self-remitting by 2 years of age.
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