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Kindler Syndrome.
Youssefian L, Vahidnezhad H, Uitto J. Youssefian L, et al. 2016 Mar 3 [updated 2022 Jan 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2016 Mar 3 [updated 2022 Jan 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 26937547 Free Books & Documents. Review.
CLINICAL CHARACTERISTICS: Kindler syndrome (KS), a rare subtype of inherited epidermolysis bullosa, is characterized by skin fragility and acral blister formation beginning at birth, diffuse cutaneous atrophy, photosensitivity (most prominent during childhood and us …
CLINICAL CHARACTERISTICS: Kindler syndrome (KS), a rare subtype of inherited epidermolysis bullosa, is characterized by skin f …
Kindler syndrome.
Lai-Cheong JE, McGrath JA. Lai-Cheong JE, et al. Dermatol Clin. 2010 Jan;28(1):119-24. doi: 10.1016/j.det.2009.10.013. Dermatol Clin. 2010. PMID: 19945624 Review.
Loss-of-function mutations in the FERMT1 gene are the cause of Kindler syndrome. Kindler syndrome is categorized as a subtype of epidermolysis bullosa (EB). ...This article reviews clinicopathologic and molecular features of Kindler syndrome …
Loss-of-function mutations in the FERMT1 gene are the cause of Kindler syndrome. Kindler syndrome is categorized …
Kindler syndrome.
Ashton GH. Ashton GH. Clin Exp Dermatol. 2004 Mar;29(2):116-21. doi: 10.1111/j.1365-2230.2004.01465.x. Clin Exp Dermatol. 2004. PMID: 14987263 Review.
Kindler syndrome is a rare, autosomal recessive skin fragility disorder characterized by blistering in infancy, followed by photosensitivity and progressive poikiloderma. ...This article reviews the clinical features as well as the molecular and cellular pathology o …
Kindler syndrome is a rare, autosomal recessive skin fragility disorder characterized by blistering in infancy, followed by ph …
Dermoscopy of Kindler Syndrome.
Neema S, Sinha P, Sandhu S, Mukherjee S, Radhakrishnan S. Neema S, et al. Dermatol Pract Concept. 2020 Apr 3;10(2):e2020034. doi: 10.5826/dpc.1002a34. eCollection 2020. Dermatol Pract Concept. 2020. PMID: 32363096 Free PMC article. No abstract available.
Kindler syndrome: a focal adhesion genodermatosis.
Lai-Cheong JE, Tanaka A, Hawche G, Emanuel P, Maari C, Taskesen M, Akdeniz S, Liu L, McGrath JA. Lai-Cheong JE, et al. Br J Dermatol. 2009 Feb;160(2):233-42. doi: 10.1111/j.1365-2133.2008.08976.x. Epub 2008 Dec 11. Br J Dermatol. 2009. PMID: 19120339 Review.
Although Kindler syndrome is classified as a subtype of epidermolysis bullosa, it has distinct clinicopathological and molecular abnormalities. ...In this report, we review the clinical, cellular and molecular pathology of Kindler syndrome and discuss …
Although Kindler syndrome is classified as a subtype of epidermolysis bullosa, it has distinct clinicopathological and molecul …
Kindler syndrome: a rare case report from Syria.
Edrees S, Jarkas N, Hraib M, Al-Yousef K, Baddour R. Edrees S, et al. Ann Med Surg (Lond). 2023 Apr 6;85(5):2077-2080. doi: 10.1097/MS9.0000000000000503. eCollection 2023 May. Ann Med Surg (Lond). 2023. PMID: 37229095 Free PMC article.
Kindler syndrome is a rare autosomal recessive inherited disease. The authors report a case with unique presentation that has never reported before in the medical Literatur" lanugo hair". This is a case of a 13-year-old Syrian child, who presented with difuse fine f …
Kindler syndrome is a rare autosomal recessive inherited disease. The authors report a case with unique presentation that has …
Epidermolysis Bullosa: Pediatric Perspectives.
Hon KL, Chu S, Leung AKC. Hon KL, et al. Curr Pediatr Rev. 2022;18(3):182-190. doi: 10.2174/1573396317666210525161252. Curr Pediatr Rev. 2022. PMID: 34036913 Review.
There are four main types: epidermolysis bullosa simplex, dystrophic epidermolysis bullosa, junctional epidermolysis bullosa, and Kindler syndrome. The diagnosis is suspected based on symptoms and confirmed by skin biopsy and definitive genetic testing. ...
There are four main types: epidermolysis bullosa simplex, dystrophic epidermolysis bullosa, junctional epidermolysis bullosa, and Kindler …
Kindler syndrome.
Sharma RC, Mahajan V, Sharma NL, Sharma AK. Sharma RC, et al. Int J Dermatol. 2003 Sep;42(9):727-32. doi: 10.1046/j.1365-4362.2003.01659.x. Int J Dermatol. 2003. PMID: 12956691
Kindler syndrome is a rare genodermatosis characterized by acral bullae and photosensitivity. ...This is the first report of such ophthalmic and skeletal features of Kindler syndrome....
Kindler syndrome is a rare genodermatosis characterized by acral bullae and photosensitivity. ...This is the first report of s …
Ocular manifestations in Kindler syndrome.
Maharana PK, Sahay P, Mandal S, Nagpal R, Sharma N. Maharana PK, et al. Indian J Ophthalmol. 2022 Jul;70(7):2585-2587. doi: 10.4103/ijo.IJO_791_22. Indian J Ophthalmol. 2022. PMID: 35791162 Free PMC article.
We aimed describe the chronic ocular sequelae of Kindler syndrome. All cases of Kindler syndrome with ocular involvement that presented to a tertiary eye care center were included. Three cases of Kindler syndrome with ocular changes were …
We aimed describe the chronic ocular sequelae of Kindler syndrome. All cases of Kindler syndrome with ocular inv …
Kindler syndrome with unique ocular findings.
Thakur A, Kulshreshtha A, Kumar S, Dogra S, Gupta A. Thakur A, et al. Indian J Ophthalmol. 2020 Jun;68(6):1182. doi: 10.4103/ijo.IJO_2261_19. Indian J Ophthalmol. 2020. PMID: 32461471 Free PMC article. No abstract available.
247 results