|1.||Has, Cristina: 7 articles (04/2015 - 11/2006)|
|2.||McGrath, John A: 7 articles (04/2014 - 07/2003)|
|3.||Has, C: 6 articles (09/2015 - 12/2006)|
|4.||Bruckner-Tuderman, Leena: 5 articles (03/2014 - 11/2006)|
|5.||Lai-Cheong, Joey E: 4 articles (04/2014 - 10/2009)|
|6.||Bruckner-Tuderman, L: 3 articles (09/2015 - 12/2007)|
|7.||McGrath, John: 3 articles (07/2015 - 11/2008)|
|8.||Fong, Kenneth: 3 articles (07/2015 - 05/2011)|
|9.||McGrath, J A: 3 articles (04/2014 - 01/2006)|
|10.||Fässler, Reinhard: 3 articles (04/2014 - 12/2008)|
10/01/1994 - "Results in our patient 2 years after correction demonstrate that syndactyly release in Kindler syndrome can be accomplished effectively, with improvement in both function and appearance."
01/01/2003 - "Syndactyly repair in Kindler syndrome."
10/01/1994 - "In this report, a patient with Kindler syndrome underwent surgical treatment of acquired syndactylies. "
10/01/1994 - "Release of acquired syndactylies in Kindler syndrome."
10/01/1994 - "Fusion of the digits secondary to blistering and scarring, "pseudosyndactyly," has been reported in several patients with Kindler syndrome; however, surgical correction of the syndactylies in these patients has not been described. "
01/01/2003 - "Clinical and microbiologic study of periodontitis associated with Kindler syndrome."
05/01/2008 - "Periodontitis in Kindler syndrome responds to maintenance therapy, but the gingiva and oral mucosa continue to display an abnormal appearance with white patches. "
01/01/2003 - "In periodontitis patients, Porphyromonas gingivallis and Diallster pneumosintes tended to occur more frequently in control individuals compared to those with Kindler syndrome. "
09/01/2012 - "In 2003, loss-of-function mutations were identified in the gene KIND1 mapped to chromosome 20p12.3. In this paper, we report Kindler syndrome in two children born to consanguineous parents presenting acral blistering, photosensitivity, poikiloderma, cutaneous atrophy and periodontitis."
|3.||Epidermolysis Bullosa Dystrophica (Dystrophic Epidermolysis Bullosa)
09/01/1997 - "The purpose of this study was to clarify the nature of the bullous component of Kindler syndrome and to determine whether this inherited skin disorder represents a variant of dystrophic epidermolysis bullosa or a unique independent clinical entity. "
03/01/2002 - "We describe a patient with Kindler syndrome with an 18-year follow-up who was initially misdiagnosed as suffering from dystrophic epidermolysis bullosa. "
09/01/1997 - "Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa."
09/01/1997 - "These results suggest that the bullous component of Kindler syndrome is distinct from dystrophic epidermolysis bullosa caused by mutations in the type VII collagen gene. "
09/01/2015 - "Kindler syndrome (KS) is a very rare genodermatosis characterized by acral blistering starting in infancy along with photosensitivity, progressive poikiloderma, cutaneous atrophy, and a variable degree of mucosal involvement. "
05/01/2012 - "Here we describe a disseminated pattern of revertant mosaicism observed in 6 patients with Kindler syndrome (KS), a genodermatosis caused by loss of kindlin-1 (encoded by FERMT1) and clinically characterized by patchy skin pigmentation and atrophy. "
09/07/2011 - "Fermitin family member 1 (FERMT1, Kindlin-1) is an epithelial-specific regulator of integrin functions and is associated with Kindler syndrome, a genetic disorder characterized by skin blistering, atrophy, and photosensitivity. "
01/01/2010 - "Kindler syndrome (KS) is a heritable skin disorder with a complex phenotype consisting of congenital skin blistering, photosensitivity, progressive generalized poikiloderma and extensive skin atrophy. "
10/01/2009 - "Kindler syndrome is an autosomal recessive disorder characterized by skin atrophy and blistering. "
01/01/2010 - "Unlike other forms of EB, Kindler syndrome is characterized by impaired actin cytoskeleton-extracellular matrix interactions and a variable plane of blister formation at or close to the dermal-epidermal junction. "
01/01/2006 - "In the family described here, molecular diagnosis of Kindler syndrome in an infant with acral blisters led to the belated diagnosis in a severely affected relative whose condition had remained unidentified for 37 years."
09/01/2003 - "Kindler syndrome is a rare genodermatosis characterized by acral bullae and photosensitivity. "
12/01/1996 - "The findings of basal layer separation in both spontaneous and induced blisters in Kindler syndrome suggest this is the true level of blister formation. "
09/01/2012 - "Kindler syndrome is a rare autosomal recessive genodermatosis characterized by trauma-induced blisters, progressive poikiloderma and varying degrees of photosensitivity. "
|1.||Poikiloderma of Kindler
|2.||collagen type XVII (collagen XVII)
|4.||Keratin-5 (Keratin 5)
|5.||Collagen Type VII
|6.||Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF)
|7.||Proteins (Proteins, Gene)
|10.||Craniosynostosis radial aplasia syndrome