Results 71 to 80 of about 12,699 (164)
Epidermolytic hyperkeratosis with Vitamin D deficiency rickets in a 5-year-old Indian girl
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
Animal Genetics, Volume 55, Issue 3, Page 490-492, June 2024.
Sarah Kiener+7 more
wiley +1 more source
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.
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.
No abstract ...
Tosti A.+4 more
openaire +3 more sources
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
Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions. [PDF]
Pondeljak N+5 more
europepmc +1 more source
Congenital Ichthyosis: A Practical Clinical Guide on Current Treatments and Future Perspectives. [PDF]
Lilly E, Bunick CG.
europepmc +1 more source
Autosomal dominant non-epidermolytic palmoplantar hyperkeratosis in a Nigerian girl
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