Results 171 to 180 of about 13,745 (220)

Mutation p.Arg127Pro in the 1A Domain of KRT16 Causes Pachyonychia Congenita in Chinese Patient: A Case Report of PC Associated with Acral Melanoma. [PDF]

Clin Cosmet Investig Dermatol
Ge WW, Chen ZM, Chou MW, Ismail F, Chen G, Wu LM, Yang JQ.   +6 more
europepmc   +1 more source

Increased risk of anxiety and coping strategies in patients with selected genodermatoses with cornification disruption. [PDF]

Sci Rep
Fryze M, Mlak R, Kulbaka A, Wertheim-Tysarowska K, Matosiuk D, Pietrzak A.   +5 more
europepmc   +1 more source

Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations. [PDF]

Genes (Basel)
Hotz A, Fölster-Holst R, Oji V, Bourrat E, Frank J, Marrakchi S, Ennouri M, Wankner L, Komlosi K, Alter S, Fischer J.   +10 more
europepmc   +1 more source

Spectrum of Inpatient Pediatric Dermatology Cases at a Tertiary Health Care Centre in South India. [PDF]

Cureus
Aiholli S, Inamadar A, Adya KA, Gore D.
europepmc   +1 more source

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Epidermolytic Hyperkeratosis in an Epidermoid (Infundibular) Cyst.

The American Journal of Dermatopathology, 2021
Epidermolytic hyperkeratosis (EHK) is an uncommon histopathologic reaction pattern that may represent a primary pathological process or a coincidental finding in a variety of neoplasms.
C. A. Prestwood, T. Vandergriff
semanticscholar   +3 more sources

Epidermal nevi and epidermolytic hyperkeratosis: A review of cases, highlighting indications for biopsy and genetics referral

Pediatric Dermatology, Volume 41, Issue 5, Page 780-785, September/October 2024.
Epidermal nevi are common benign cutaneous hamartomas that may rarely demonstrate histopathologic evidence of epidermolytic hyperkeratosis (EHK), representing cutaneous mosaicism for pathogenic keratin variants.
Jessie M Nelson, Jacqueline M Isaac, Julie E. Mervak, Jennifer B. Mancuso, May P Chan, Amanda Arreola, K. B. Cha   +6 more
semanticscholar   +2 more sources

Epidermolytic Hyperkeratosis.

JAMA Dermatology, 2021
M. Foster, Jordan M. Jones, C. Schadt
semanticscholar   +3 more sources

Two cases of KRT1 mutation‐associated epidermolytic ichthyosis without typical epidermolytic hyperkeratosis in the neonatal skin lesions

Pediatric dermatology, 2023
Epidermolytic ichthyosis (EI) is a rare genetic disorder of keratinization caused by mutations in either KRT1 or KRT10. Histopathologically, epidermolytic hyperkeratosis (EHK) is a hallmark of EI.
Taehee Kim, Soo-Chan Kim, S. E. Lee
semanticscholar   +1 more source