eMedicine Specialties > Dermatology > Pediatric Diseases
Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma): Multimedia
Updated: Jan 24, 2007
Multimedia
![]() | Media file 1: Anterior ankles. |
![]() | Media file 2: Close-up view of ankle. |
![]() | Media file 3: Pathology of epidermolytic hyperkeratosis (hematoxylin and eosin stain). |
![]() | Media file 4: Pathology of epidermolytic hyperkeratosis (hematoxylin and eosin stain). |
More on Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma) |
| Overview: Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma) |
| Differential Diagnoses & Workup: Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma) |
| Treatment & Medication: Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma) |
| Follow-up: Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma) |
Multimedia: Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma) |
| References |
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References
Bale SJ, DiGiovanna JJ. Genetic approaches to understanding the keratinopathies. Adv Dermatol. 1997;12:99-113; discussion 114. [Medline].
DiGiovanna JJ, Bale SJ. Clinical heterogeneity in epidermolytic hyperkeratosis. Arch Dermatol. Aug 1994;130(8):1026-35. [Medline].
Kragballe K, Steijlen PM, Ibsen HH, et al. Efficacy, tolerability, and safety of calcipotriol ointment in disorders of keratinization. Results of a randomized, double-blind, vehicle-controlled, right/left comparative study. Arch Dermatol. May 1995;131(5):556-60. [Medline].
Kwak J, Maverakis E. Epidermolytic hyperkeratosis. Dermatol Online J. 2006;12(5):6. [Medline].
Lacz NL, Schwartz RA, Kihiczak G. Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event. Int J Dermatol. Jan 2005;44(1):1-6. [Medline].
Leigh IM, Lane EB. Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis. Arch Dermatol. Dec 1993;129(12):1571-7. [Medline].
Math A, Frank J, Handisurya A, et al. Identification of a de novo keratin 1 mutation in epidermolytic hyperkeratosis with palmoplantar involvement. Eur J Dermatol. Sep-Oct 2006;16(5):507-10. [Medline].
McGowan KA, Aradhya S, Fuchs H, et al. A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis. J Invest Dermatol. May 2006;126(5):1013-6. [Medline].
Muller FB, Huber M, Kinaciyan T, et al. A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis. Hum Mol Genet. Apr 1 2006;15(7):1133-41. [Medline].
Rothnagel JA, Lin MT, Longley MA, et al. Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis. Prenat Diagn. Aug 1998;18(8):826-30. [Medline].
Smack DP, Korge BP, James WD. Keratin and keratinization. J Am Acad Dermatol. Jan 1994;30(1):85-102. [Medline].
Further Reading
Keywords
bullous congenital ichthyosiform erythroderma








Multimedia: Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma)