Arrhythmogenic cardiomyopathy.
Pilichou K, Thiene G, Bauce B, Rigato I, Lazzarini E, Migliore F, Perazzolo Marra M, Rizzo S, Zorzi A, Daliento L, Corrado D, Basso C.
Orphanet J Rare Dis. 2016 Apr 2;11:33. doi: 10.1186/s13023-016-0407-1.
Desmosomal genodermatoses.
Petrof G, Mellerio JE, McGrath JA.
Br J Dermatol. 2012 Jan;166(1):36-45. doi: 10.1111/j.1365-2133.2011.10640.x.
Treatment of hereditary palmoplantar keratoderma: a review by analysis of the literature.
Bodemer C, Steijlen P, Mazereeuw-Hautier J, O'Toole EA.
Br J Dermatol. 2021 Mar;184(3):393-400. doi: 10.1111/bjd.19144. Epub 2020 Jun 17.
Hidrotic Ectodermal Dysplasia 2.
Mellerio J, Greenblatt D.
2005 Apr 25 [updated 2025 Apr 3]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
CEDNIK syndrome with phenotypic variability.
Nanda A, Karam TM, AlLafi A.
Pediatr Dermatol. 2022 Jul;39(4):650-652. doi: 10.1111/pde.14961. Epub 2022 Mar 1.
Desmoplakin mutations with palmoplantar keratoderma, woolly hair and cardiomyopathy.
Pigors M, Schwieger-Briel A, Cosgarea R, Diaconeasa A, Bruckner-Tuderman L, Fleck T, Has C.
Acta Derm Venereol. 2015 Mar;95(3):337-40. doi: 10.2340/00015555-1974.
Nonsyndromic Hearing Loss and Deafness, Mitochondrial.
Usami SI, Nishio SY.
2004 Oct 22 [updated 2018 Jun 14]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
Pain mechanisms in hereditary palmoplantar keratodermas.
Weinberg RL, Coulombe PA, Polydefkis M, Caterina MJ.
Br J Dermatol. 2020 Mar;182(3):543-551. doi: 10.1111/bjd.17880. Epub 2019 Jul 24.
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas.
Stevens HP, Kelsell DP, Bryant SP, Bishop DT, Spurr NK, Weissenbach J, Marger D, Marger RS, Leigh IM.
Arch Dermatol. 1996 Jun;132(6):640-51.
Olmsted syndrome: clinical, molecular and therapeutic aspects.
Duchatelet S, Hovnanian A.
Orphanet J Rare Dis. 2015 Mar 17;10:33. doi: 10.1186/s13023-015-0246-5.
