Literature DB >> 23091584

Ichthyosis bullosa of Siemens.

Charlene U Ang-Tiu1, Marie Eleanore O Nicolas.   

Abstract

BACKGROUND: Ichthyosis bullosa of Siemens (IBS) is a rare hyperkeratotic blistering condition caused by mutations in keratin 2e gene. MAIN OBSERVATIONS: This is a case of a 18-year-old female with generalized blisters, erosions and thickened skin since she was 3 months old. As she aged, there was decrease in development of blisters and erosions, with accompanying increase in severity of hyperkeratosis. Skin punch biopsy showed overlying basket weave hyperkeratosis and acanthosis, prominent vacuolization of the granular cell layer, and intraepidermal blisters with the split at the granular layer. The patient was treated with emollients, with marked improvement.
CONCLUSIONS: Mutations in the different keratin genes have been shown to underlie a wide range of disorders of keratinization. Epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens are distinct disorders with mutations in different genes. Although molecular genetic testing should ideally be done for confirmation of diagnosis, ichthyosis bullosa of Siemens could be diagnosed in this patients based on key clinical characteristics.

Entities:  

Keywords:  epidermolytic hyperkeratosis; ichthyosis bullosa of Siemens

Year:  2012        PMID: 23091584      PMCID: PMC3470794          DOI: 10.3315/jdcr.2012.1107

Source DB:  PubMed          Journal:  J Dermatol Case Rep        ISSN: 1898-7249


  10 in total

Review 1.  The keratins and their disorders.

Authors:  Elizabeth L Rugg; Irene M Leigh
Journal:  Am J Med Genet C Semin Med Genet       Date:  2004-11-15       Impact factor: 3.908

Review 2.  Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event.

Authors:  Nicole L Lacz; Robert A Schwartz; George Kihiczak
Journal:  Int J Dermatol       Date:  2005-01       Impact factor: 2.736

3.  A sporadic case of epidermolytic hyperkeratosis caused by a novel point mutation in the keratin 1 gene.

Authors:  Y Shimomura; N Sato; K Tomiyama; A Takahashi; M Ito
Journal:  Clin Exp Dermatol       Date:  2006-03       Impact factor: 3.470

Review 4.  The molecular genetics of keratin disorders.

Authors:  Frances Smith
Journal:  Am J Clin Dermatol       Date:  2003       Impact factor: 7.403

5.  Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.

Authors:  V P Sybert; J S Francis; L D Corden; L T Smith; M Weaver; K Stephens; W H McLean
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

Review 6.  Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature.

Authors:  T Basarab; F J Smith; V M Jolliffe; W H McLean; S Neill; M H Rustin; R A Eady
Journal:  Br J Dermatol       Date:  1999-04       Impact factor: 9.302

7.  Epidermolytic hyperkeratosis type NPS-3: a case report.

Authors:  Asja Prohić; Almira Selmanagić; Nurija Bilalović
Journal:  Acta Dermatovenerol Croat       Date:  2007       Impact factor: 1.256

Review 8.  New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.

Authors:  N V Whittock; G H Ashton; W A Griffiths; R A Eady; J A McGrath
Journal:  Br J Dermatol       Date:  2001-08       Impact factor: 9.302

Review 9.  Ichthyosis bullosa of Siemens: its correct diagnosis facilitated by molecular genetic testing.

Authors:  M Akiyama; Y Tsuji-Abe; M Yanagihara; K Nakajima; H Kodama; M Yaosaka; M Abe; D Sawamura; H Shimizu
Journal:  Br J Dermatol       Date:  2005-06       Impact factor: 9.302

10.  Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5.

Authors:  Eli Sprecher; Gil Yosipovitch; Reuven Bergman; Dan Ciubutaro; Margarita Indelman; Ellen Pfendner; Leok C Goh; Christopher J Miller; Jouni Uitto; Gabriele Richard
Journal:  J Invest Dermatol       Date:  2003-04       Impact factor: 8.551

  10 in total
  1 in total

Review 1.  Settling the score: variant prioritization and Mendelian disease.

Authors:  Karen Eilbeck; Aaron Quinlan; Mark Yandell
Journal:  Nat Rev Genet       Date:  2017-08-14       Impact factor: 53.242

  1 in total

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