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Page 1
Vohwinkel Syndrome.
Saleh D, Saleh HM, Tanner LS. Saleh D, et al. 2023 Nov 13. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. 2023 Nov 13. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan–. PMID: 30335335 Free Books & Documents.
Vohwinkel syndrome, also known as keratoderma hereditarian mutilans, is classified as a type of hereditary palmoplantar keratoderma (PPK). ...A variant of Vohwinkel syndrome, loricrin keratoderma, presents as a honeycomb PPK with pseudoai …
Vohwinkel syndrome, also known as keratoderma hereditarian mutilans, is classified as a type of hereditary palmoplantar …
Mutilating keratoderma of Vohwinkel.
Reddy BS, Gupta SK. Reddy BS, et al. Int J Dermatol. 1983 Nov;22(9):530-3. doi: 10.1111/j.1365-4362.1983.tb02196.x. Int J Dermatol. 1983. PMID: 6227573 No abstract available.
Vohwinkel syndrome: treatment of pseudo-ainhum.
Bassetto F, Tiengo C, Sferrazza R, Belloni-Fortina A, Alaibac M. Bassetto F, et al. Int J Dermatol. 2010 Jan;49(1):79-82. doi: 10.1111/j.1365-4632.2009.04267.x. Int J Dermatol. 2010. PMID: 20465619
BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar keratosis which manifests in infants and becomes more evident in adulthood. ...RESULTS AND CONCLUSION: In this study, we present an additional case of …
BACKGROUND: Vohwinkel syndrome or keratoderma hereditaria mutilans is a rare autosomal dominant palmoplantar keratosis …
An Indian case of keratoderma hereditarium mutilans (Vohwinkel's syndrome) associated with ichthyosiform dermatosis.
Vijaikumar M, Thappa DM, Jeevankumar B. Vijaikumar M, et al. J Dermatol. 2001 Oct;28(10):560-3. doi: 10.1111/j.1346-8138.2001.tb00031.x. J Dermatol. 2001. PMID: 11732725
Keratoderma hereditarium mutilans (KHM) or Vohwinkel's syndrome (VS) is usually inherited as an autosomal dominant disease, but a recessive type has occasionally been described. ...On examination, his generalized ichthyosiform dermatosis was accompanied by se …
Keratoderma hereditarium mutilans (KHM) or Vohwinkel's syndrome (VS) is usually inherited as an autosomal dominant dise …
Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis).
Schmuth M, Fluhr JW, Crumrine DC, Uchida Y, Hachem JP, Behne M, Moskowitz DG, Christiano AM, Feingold KR, Elias PM. Schmuth M, et al. J Invest Dermatol. 2004 Apr;122(4):909-22. doi: 10.1111/j.0022-202X.2004.22431.x. J Invest Dermatol. 2004. PMID: 15102081 Free article.
In contrast, insertional mutations resulting in a frameshift in the C-terminal domain of loricrin produce the characteristic ichthyosis of loricrin keratoderma in mouse and man. To ascertain the basis for the loricrin keratoderma phenotype, we assessed epidermal str …
In contrast, insertional mutations resulting in a frameshift in the C-terminal domain of loricrin produce the characteristic ichthyosis of l …
Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin.
Camisa C, Rossana C. Camisa C, et al. Arch Dermatol. 1984 Oct;120(10):1323-8. Arch Dermatol. 1984. PMID: 6237617
Keratoderma hereditaria mutilans (KHM), or Vohwinkel's syndrome, is a rare genodermatosis consisting of hyperkeratosis of the palms and soles with a characteristic "honeycomb" appearance, keratotic structures taking the shape of a starfish and/or knuckle pads …
Keratoderma hereditaria mutilans (KHM), or Vohwinkel's syndrome, is a rare genodermatosis consisting of hyperkeratosis …
Keratoderma hereditaria mutilans (vohwinkel's syndrome).
Dayal S, Jain VK, Singh H. Dayal S, et al. Indian J Dermatol Venereol Leprol. 1997 May-Jun;63(3):186-8. Indian J Dermatol Venereol Leprol. 1997. PMID: 20944319
We report two cases of Vohwinkel's syndrome in son and mother presenting with a progressive palmoplantar keratoderma with 'honeycomb' appearance associated with constricting bands encircling digits of hands and feet along with keratotic plaques on dors …
We report two cases of Vohwinkel's syndrome in son and mother presenting with a progressive palmoplantar keratoderma …
Loricrin keratoderma: a novel disease entity characterized by nuclear accumulation of mutant loricrin.
Ishida-Yamamoto A. Ishida-Yamamoto A. J Dermatol Sci. 2003 Feb;31(1):3-8. doi: 10.1016/s0923-1811(02)00143-3. J Dermatol Sci. 2003. PMID: 12615358 Review.
Clinically, these patients can be diagnosed as suffering from an ichthyotic variant of Vohwinkel's syndrome (VS), progressive symmetric erythrokeratoderma, or congenital ichthyosiform erythroderma born as a collodion baby. ...This group of unique genodermatoses caus …
Clinically, these patients can be diagnosed as suffering from an ichthyotic variant of Vohwinkel's syndrome (VS), progressive …
Keratoderma hereditaria mutilans (Vohwinkel's syndrome): a trial of isotretinoin.
Goldfarb MT, Woo TY, Rasmussen JE. Goldfarb MT, et al. Pediatr Dermatol. 1985 Mar;2(3):216-8. doi: 10.1111/j.1525-1470.1985.tb01056.x. Pediatr Dermatol. 1985. PMID: 3157929 Free article.
An 8-year-old girl with the classic findings of keratoderma hereditaria mutilans (Vohwinkel's syndrome) was seen. Treatment with isotretinoin was instituted to decrease the hyperkeratosis and to prevent further autoamputation. ...
An 8-year-old girl with the classic findings of keratoderma hereditaria mutilans (Vohwinkel's syndrome) was seen. Treat …
The Epidermal Transcriptome Analysis of a Novel c.639_642dup LORICRIN Variant-Delineation of the Loricrin Keratoderma Pathology.
Wertheim-Tysarowska K, Osipowicz K, Gielniewski B, Wojtaś B, Szabelska-Beręsewicz A, Zyprych-Walczak J, Mika A, Tysarowski A, Duk K, Rygiel AM, Niepokój K, Woźniak K, Kowalewski C, Wierzba J, Jezela-Stanek A. Wertheim-Tysarowska K, et al. Int J Mol Sci. 2023 May 29;24(11):9459. doi: 10.3390/ijms24119459. Int J Mol Sci. 2023. PMID: 37298411 Free PMC article.
Loricrin keratoderma (LK) is a rare autosomal dominant genodermatosis caused by LORICRIN gene mutations. ...We also present the results of the transcriptome analysis of the lesional loricrin keratoderma epidermis of a patient with c.639_642dup. We show that in the L …
Loricrin keratoderma (LK) is a rare autosomal dominant genodermatosis caused by LORICRIN gene mutations. ...We also present the resul …
100 results