Results 61 to 70 of about 3,156 (181)

Epidermolysis bullosa in practice of dermatologist [PDF]

Саратовский научно-медицинский журнал, 2014
This article describes a clinical case of a rare dermatosis — congenital dystrophic epidermolysis bullosa in a 9-year old child.
Shustova О.А., Bobko N.К.
doaj  

Epidermolysis Bullosa: Two rare case reports of COL7A1 and EBS-GEN SEV KRT14 variants with review of literature

BMC Pediatrics
Epidermolysis Bullosa is a rare hereditary skin condition that causes blisters. Genes encoding structural proteins at or near the dermal-epidermal junction are mutated recessively or dominantly, and this is the primary cause of EB.
Fatma Mabrouk Ali, Jieyu Zhou, Mingyan Wang, Qiuxia Wang, Lulu Sun, Mansour Maulid Mshenga, Hongyan Lu   +6 more
doaj   +1 more source

Recessive dystrophic epidermolysis bullosa. [PDF]

Anaesthesia, 1983
Summary A case report is presented of a patient with recessive dystrophic epidermolysis bullosa requiring anaesthesia for thoraco‐abdominal surgery. The classification and pathology of epidermolysis bullosa is considered together with the clinical features and treatment.
openaire   +2 more sources

Preimplantation Genetic Diagnosis for DEB by Detecting a Novel Family-Specific COL7A1 Mutation in Vietnam

The Application of Clinical Genetics, 2021
Sang Trieutien,1,* Tam Vu Van,2,3,* My Tran Ngoc Thao,4 Son Trinh The,5 Khoa Tran Van,1 Tung Nguyen Thanh,5 Tuan Tran Van,5 Hanh Nguyen Thi6 1Department of Biology and Genetics, Vietnam Military Medical University, Hanoi, 12108, Vietnam ...
Trieutien S, Vu Van T, Tran Ngoc Thao M, Trinh The S, Tran Van K, Nguyen Thanh T, Tran Van T, Nguyen Thi H   +7 more
doaj  

Dystrophic Epidermolysis Bullosa [PDF]

Journal of Perinatology, 2003
Bibhuti B, Das, Sunati, Sahoo
openaire   +2 more sources

Expression of Integrins in Junctional and Dystrophic Epidermolysis Bullosa

Journal of Investigative Dermatology, 1990
Recently, monoclonal antibodies (MoAb) have been raised against a family of adhesive membrane receptors (R) for extracellular matrix molecules known as integrins. In order to ascertain whether these adhesive proteins are normally expressed in inherited epidermolysis bullosa (EB) dermal epidermal junction, we studied the reactivity of MoAb recognizing ...
V. Nazzaro, E. Berti, A. Cerri, A. Brusasco, R. Cavalli, R. Caputo   +5 more
openaire   +3 more sources

Ex Vivo COL7A1 Correction for Recessive Dystrophic Epidermolysis Bullosa Using CRISPR/Cas9 and Homology-Directed Repair

Molecular Therapy: Nucleic Acids, 2018
Recessive dystrophic epidermolysis bullosa is a rare and severe genetic skin disease resulting in blistering of the skin and mucosa. Recessive dystrophic epidermolysis bullosa (RDEB) is caused by a wide variety of mutations in COL7A1-encoding type VII ...
Araksya Izmiryan, Clarisse Ganier, Matteo Bovolenta, Alain Schmitt, Fulvio Mavilio, Alain Hovnanian   +5 more
doaj   +1 more source

Nail Dystrophy Treated With Marigold Therapy in a Patient With Epidermolysis Bullosa Simplex

Australasian Journal of Dermatology, Volume 67, Issue 4, Page e255-e256, June 2026.
Aalia Syed, M. Tariq Khan, Dédée F. Murrell   +2 more
wiley   +1 more source

The tumor microenvironment of cutaneous squamous cell carcinoma in high-risk patient groups: A scoping review

JID Innovations
Cutaneous squamous cell carcinoma (cSCC) is a prevalent skin cancer in the general population that poses so far unresolved challenges in high-risk groups such as organ transplant recipients and individuals with recessive dystrophic epidermolysis bullosa.
Wandong Wang, Clara Harrs, Maria C. Bolling, Barbara Horváth, Gilles F.H. Diercks, Emőke Rácz   +5 more
doaj   +1 more source

Glomerulonephritis in Youth With Dystrophic Epidermolysis Bullosa [PDF]

Kidney International Reports, 2021
Erica Hughley, Edward J. Nehus, Katherine VandenHeuvel, Bret D. Augsburger, Namrata G. Jain, Anne W. Lucky   +5 more
openaire   +3 more sources