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Unusual oral manifestation of Kindler syndrome: a case report and review of literature.
Front Oral Health
September 2024
Department of Oral and Maxillofacial Surgery, A B Shetty Memorial Institute of Dental Sciences, Nitte (Deemed to be University), Deralakatte, India.
Article Synopsis
- Kindler syndrome (KS) is a rare skin condition that starts in babies and causes painful blisters, unusual skin color changes, and sensitivity to sunlight as they get older.
- It happens because of a problem with a protein called kindlin-1, which helps skin cells stick together and move properly.
- People with KS can have issues with their mouths that are often missed or treated wrong, and having diabetes can make these problems worse, leading to bigger challenges with healing and skin issues.
Orofacial Manifestations of Kindler Epidermolysis Bullosa.
JAMA Dermatol
October 2024
Schulich School of Medicine and Dentistry, Western University, London, Ontario, Canada.
Epidemiological Characteristics of Inherited Epidermolysis Bullosa in an Eastern European Population.
J Clin Med
June 2024
Pediatric Dermatology Discipline, Carol Davila University of Medicine and Pharmacy, 8 Eroilor Sanitari Boulevard, 050474 Bucharest, Romania.
: Epidermolysis bullosa (EB) is a hereditary condition characterized by skin and mucosal fragility, with various degrees of severity. This study's objectives are to obtain updated epidemiological data that will help identify the specific types and subtypes of EB, determine the case distribution in Romania, and establish the incidence and prevalence of the condition. : This population-based observational study included Romanian patients and collected data from 2012 to 2024.
View Article and Find Full Text PDFA 1.9 mm Trilogy lithotripter in mini percutaneous nephrolithotomy Description of technique and case outcomes.
Can Urol Assoc J
November 2024
New York Medical College, Valhalla NY, United States.
Introduction: We aimed to evaluate the novel use of a 1.9 mm Trilogy lithotripter probe with varying locations and composition of renal stones.
Methods: We prospectively enrolled patients to undergo mini percutaneous nephrolithotomy (mPCNL) procedures using the 1.
Dermoscopic Correlation of an Eccentric Case of Kindler Syndrome.
Cureus
April 2024
Dermatology, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune, IND.
Article Synopsis
- - Kindler syndrome (KS) is a rare genetic skin disorder caused by mutations in the FERMT1 gene, leading to blistering, epidermal atrophy, increased cancer risk, and poor wound healing.
- - A 20-something male patient experienced symptoms like hyper-hypopigmentation, facial poikiloderma, thin wrinkled skin, and childhood blistering that left atrophic scars.
- - The study aims to link clinical findings with dermoscopy, highlighting its effectiveness in diagnosing KS through the identification of key features like poikiloderma and unique scar types.
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