Síndrome de Kindler, manejo multidisciplinario
Author:
Publisher
Elsevier BV
Subject
Dermatology,Histology,Pathology and Forensic Medicine
Reference18 articles.
1. Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy;Kindler;Br J Dermatol.,1954
2. The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB;Fine;J Am Acad Dermatol.,2008
3. Kindler syndrome;Youssefian,2016
4. Epidermolysis bullosa in Perú: clinical and epidemiological study of patients treated in a national reference pediatric hospital, 1993-2015;Torres-Iberico;Rev Peru Med Exp Salud Pública.,2017
5. Kindler syndrome: Extension of FERMT1 mutational spectrum and natural history;Has;Hum Mutat.,2011
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1. Identification of a novel FERMT1 variant causing kindler syndrome and a review of the clinical and molecular genetic features in Chinese patients;Frontiers in Pediatrics;2024-09-06
2. Battling a rarity: A case of kindler syndrome from a developing country;SAGE Open Medical Case Reports;2024-01
3. Epidermolysis Bullosa—A Kindler Syndrome Case Report and Short Literature Review;Clinics and Practice;2023-07-30
4. Kindler syndrome: a rare case report from Syria;Annals of Medicine & Surgery;2023-04-07
5. Kindler syndrome and role of dental surgeon: Providing quality oral health care – A case report;SRM Journal of Research in Dental Sciences;2023
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