Results 71 to 80 of about 12,699 (164)

Epidermolytic hyperkeratosis with Vitamin D deficiency rickets in a 5-year-old Indian girl

open access: yes, 2015
We report a 5-year-old child with hyperkeratotic lesions over upper and lower limbs, with bowing of legs and limping. It was proved to be epidermolytic hyperkeratosis (EHK) with nutritional rickets on the basis of clinical, biochemical, radiological and ...
A. Roy, Debalina Sarkar, P. Dey, S. Pal
semanticscholar   +1 more source

Heterozygous ASPRV1 frameshift variant in a Pembroke Welsh Corgi with ichthyosis

open access: yes
Animal Genetics, Volume 55, Issue 3, Page 490-492, June 2024.
Sarah Kiener   +7 more
wiley   +1 more source

Hiperqueratose palmo-plantar epidermolítica (Vörner) relato de caso e revisão da literatura Epidermolytic palmoplantar keratoderma (Vörner type) case report and revision of literature

open access: yesAnais Brasileiros de Dermatologia, 2002
As queratodermias palmo-plantares familiares são doenças pouco comuns. As manifestações clínicas são variadas e exuberantes, atraindo a atenção dos dermatologistas.
Alexandre Bortoli Machado   +4 more
doaj   +1 more source

Genetic Bases of Epidermolysis Bullosa Simplex and Epidermolytic Hyperkeratosis.

open access: yesJournal of Investigative Dermatology, 1994
Keratins are the major structural proteins of the epidermis. Analyzing keratin gene sequences, appreciating the switch in keratin gene expression that takes place as epidermal cells commit to terminally differentiate, and elucidating how keratins assemble into 10-nm filaments have provided the foundation that has led to the discoveries of the genetic ...
Andrew J. Syder   +9 more
openaire   +3 more sources

Epidermolytic hyperkeratosis of the nails in keratosis palmoplantaris nummularis.

open access: yesActa Dermato-Venereologica, 1995
No abstract ...
Tosti A.   +4 more
openaire   +3 more sources

Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family

open access: yesTherapeutics and Clinical Risk Management, 2014
Zhiliang Li,1,* Qiao Liu,2,* Aimin Wang,2 Hongsheng Wang,1 Chengrang Li1 1Department of Dermatology, Institute of Dermatology, Chinese Academy of Medical Sciences and Peking Union Medical College, Nanjing, People's Republic of China; 2Hainan ...
Li Z, Liu Q, Wang A, Wang H, Li C
doaj  

Autosomal dominant non-epidermolytic palmoplantar hyperkeratosis in a Nigerian girl

open access: yesNigerian Journal of Paediatrics
Palmoplantar keratoderma (PPK) is a hereditary cutaneous disorder characterized by a marked hyperkeratosis of the palms and soles. A variant that was inherited in an autosomal dominant form was highlighted in a 20-month-old girl-child.
Anigilaje EA, Dzuachii DO
doaj  

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