Kindler-Syndrom
Author:
Publisher
Springer Science and Business Media LLC
Subject
Dermatology
Link
http://link.springer.com/content/pdf/10.1007/s00105-008-1676-y.pdf
Reference14 articles.
1. Penagos H, Jaen M, Sancho MT et al (2004) Kindler syndrome in native Americans from Panama: report of 26 cases. Arch Dermatol 140:939–944
2. Siegel DH, Ashton GH, Penagos HG et al (2003) Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Am J Hum Genet 73:174–187
3. Lai-Cheong JE, Tanaka A, Hawche G et al (2008) Kindler syndrome: a focal adhesion genodermatosis. Br J Dermatol 160:233–242
4. Fine JD, Eady RA, Bauer EA et al (2008) The classification of inherited epidermolysis bullosa (EB): report of the Third International Consensus Meeting on Diagnosis and Classification of EB. J Am Acad Dermatol 58:931–950
5. Mansur AT, Elcioglu NH, Aydingoz IE et al (2007) Novel and recurrent KIND1 mutations in two patients with Kindler syndrome and severe mucosal involvement. Acta Derm Venereol 87:563–565
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1. Oral manifestations and their management in Kindler's syndrome: An oral clinician's perspective;Oral Science International;2023-07-04
2. Literatur;Atlas der Pädiatrischen Dermatologie;2018-07-11
3. Oral manifestations in Kindler syndrome: case report and discussion of literature findings;Special Care in Dentistry;2016-01-27
4. Kindler syndrome - a rare type of hereditary epidermolysis bullosa;Vestnik dermatologii i venerologii;2015-08-24
5. Epidermolysis bullosa;Atlas of Genodermatoses, Second Edition;2015-06-25
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