5
Views
0
CrossRef citations to date
0
Altmetric
Correspondence

Dorfman–Chanarin syndrome with cirrhosis

, , , &
Pages 650-653 | Published online: 06 Jul 2009

  • Judge M R, McLean W H, Munro C S. Disorders of keratinization. Rook's Textbook of Dermatology. 7th ed, T Burns, S Breathnach, N Cox, C Griffiths. Blackwell Science, Oxford 2004; 34: 1–111
  • Gandhi V, Aggarwal P, Dhawan J, Singh U R, Bhattacharya S N. Dorfman-Chanarin syndrome. Indian J Dermatol Venereol Leprol 2007; 73: 36–39
  • Duzovali O, Ikizoglu G, Turhan A H, Yilgor E. Dorfman-Chanarin syndrome: a case with hyperlipidemia. Turk J Pediatr 2006; 48: 263–265
  • Taskin E, Akarsu S, Aygun A D, Ozlu F, Kilic M. Rickets with Dorfman-Chanarin syndrome. Acta Haematol 2007; 117: 16–19
  • Wollenberg A, Geiger E, Schaller M, Wolff H. Dorfman-Chanarin syndrome in a Turkish kindred: conductor diagnosis requires analysis of multiple eosinophils. Acta Derm Venereol 2000; 80: 39–43
  • Pujol R M, Gilaberte M, Toll A, et al. Erythrokeratoderma variabilis-like ichthyosis in Chanarin-Dorfman syndrome. Br J Dermatol 2005; 153: 838–841
  • Tavian D, Colombo R. Improved cytochemical method for detecting Jordans' bodies in neutral-lipid storage diseases. J Clin Pathol 2007; 60: 956–958
  • Gupta P, Kaur G. Chanarin Dorfman syndrome neonatal diagnosis and 3-year follow-up. Indian Pediatr 2005; 42: 1054–1055
  • Kaassis C, Ginies J L, Berthelot J, Verret J L. Dorfman-Chanarin syndrome. Ann Dermatol Venereol 1998; 125: 317–319
  • Demerjian M, Crumrine D A, Milstone L M, Williams M L, Elias P M. Barrier dysfunction and pathogenesis of neutral lipid storage disease with ichthyosis (Chanarin-Dorfman syndrome). J Invest Dermatol 2006; 126: 2032–2038
  • Wolf R, Zaritzky A, Pollak S. Value of looking at leukocytes in every case of ichthyosis. Dermatologica 1988; 177: 237–240
  • Dorfman M L, Hershko C, Eisenberg S, Sagher F. Ichthyosiform dermatosis with systemic lipidosis. Arch Dermatol 1974; 110: 261–266
  • Yamaguchi T, Omatsu N, Matsushita S, Osumi T. CGI-58 interacts with perilipin and is localized to lipid droplets. Possible involvement of CGI-58 mislocalization in Chanarin-Dorfman syndrome. J Biol Chem 2004; 279: 30490–30497
  • Lass A, Zimmermann R, Haemmerle G, et al. Adipose triglyceride lipase-mediated lipolysis of cellular fat stores is activated by CGI-58 and defective in Chanarin-Dorfman Syndrome. Cell Metab 2006; 3: 309–319
  • Tullu M S, Muranjan M N, Save S U, Deshmukh C T, Khubchandani S R, Bharucha B A. Dorfman-Chanarin syndrome: A rare neutral lipid storage disease. Indian Pediatr 2000; 37: 88–93
  • Judge M R, Atherton D J, Salvayre R, et al. Neutral lipid storage disease: Case report and lipid studies. Br J Dermatol 1994; 130: 507–510
  • Srebrnik A, Tur E, Perluk C, et al. Dorfman-Chanarin syndrome: A case report and a review. J Am Acad Dermatol 1987; 17: 801–808
  • Amarapurkar A D, Kher A, Agrawal R, Meenakshi B, Kandalkar B M, Deshpande J R. A rare cause of steatohepatitis. Trop Gastroenterol 2004; 25: 176–177
  • Srinivasan R, Hadzic N, Fischer J, Knisely A S. Steatohepatitis and unsuspected micronodular cirrhosis in Dorfman-Chanarin syndrome with documented ABHD5 mutation. J Pediatr 2004; 144: 662–665
  • Nanda A, Sharma R, Kanwar A J, Kaur S, Dash S. Dorfman-Chanarin syndrom. Int J Dermatol 1990; 29: 349–351

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.