Literature DB >> 6237617

Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin.

C Camisa, C Rossana.   

Abstract

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 on the dorsal surfaces of the hands, and constricting bands (pseudoainhum) encircling digits of the hands and feet. We describe three cases of a variant of KHM with an associated ichthyosiform dermatosis in a pedigree consisting of 19 affected individuals through six generations. An autosomal dominant inheritance pattern for KHM was confirmed. One of the patients was successfully treated with isotretinoin, 0.6 mg/kg/day orally. We offer five hypothetical genetic models to account for the simultaneous expression of palmar-plantar keratoderma and ichthyosiform dermatosis.

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Year:  1984        PMID: 6237617

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  10 in total

1.  The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope.

Authors:  A Ishida-Yamamoto; J A McGrath; H Lam; H Iizuka; R A Friedman; A M Christiano
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

Review 2.  Ichthyosis update: towards a function-driven model of pathogenesis of the disorders of cornification and the role of corneocyte proteins in these disorders.

Authors:  Matthias Schmuth; Robert Gruber; Peter M Elias; Mary L Williams
Journal:  Adv Dermatol       Date:  2007

Review 3.  The retinoids. A review of their clinical pharmacology and therapeutic use.

Authors:  C E Orfanos; R Ehlert; H Gollnick
Journal:  Drugs       Date:  1987-10       Impact factor: 9.546

4.  Suppressing AP1 factor signaling in the suprabasal epidermis produces a keratoderma phenotype.

Authors:  Ellen A Rorke; Gautam Adhikary; Christina A Young; Dennis R Roop; Richard L Eckert
Journal:  J Invest Dermatol       Date:  2014-08-22       Impact factor: 8.551

5.  Transgenic mice expressing a mutant form of loricrin reveal the molecular basis of the skin diseases, Vohwinkel syndrome and progressive symmetric erythrokeratoderma.

Authors:  Y Suga; M Jarnik; P S Attar; M A Longley; D Bundman; A C Steven; P J Koch; D R Roop
Journal:  J Cell Biol       Date:  2000-10-16       Impact factor: 10.539

6.  A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma.

Authors:  V A Kinsler; S Drury; A Khan; R Waelchli; G Rukaite; A Barnicoat; N Lench; J I Harper; R F L O'Shaughnessy
Journal:  Br J Dermatol       Date:  2014-12-09       Impact factor: 9.302

7.  Novel autosomal dominant mutation in loricrin presenting as prominent ichthyosis.

Authors:  E Pohler; F Cunningham; A Sandilands; C Cole; S Digby; J R McMillan; S Aristodemou; J A McGrath; F J D Smith; W H I McLean; C S Munro; M Zamiri
Journal:  Br J Dermatol       Date:  2015-08-22       Impact factor: 9.302

Review 8.  Diagnosis and Management of Inherited Palmoplantar Keratodermas.

Authors:  Bjorn R Thomas; Edel A O'Toole
Journal:  Acta Derm Venereol       Date:  2020-03-25       Impact factor: 3.875

9.  Vohwinkel's Syndrome: A Rare Disorder of Keratinization.

Authors:  Nidhi Choudhary; Rahul Ahar; Abhishek De; Projna Biswas
Journal:  Indian J Dermatol       Date:  2014-11       Impact factor: 1.494

10.  Using a Distant Abdominal Skin Flap to Treat Digital Constriction Bands: A Case Report for Vohwinkel Syndrome.

Authors:  Mingzi Zhang; Kexin Song; Ning Ding; Chang Shu; Youbin Wang
Journal:  Medicine (Baltimore)       Date:  2016-02       Impact factor: 1.817

  10 in total

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