Literature DB >> 11422044

A case of Rombo syndrome.

M A van Steensel1, N G Jaspers, P M Steijlen.   

Abstract

Rombo syndrome is a rare entity characterized by the presence of atrophoderma vermiculatum of the face, multiple milia, telangiectases, acral erythema and a propensity to develop basal cell carcinomas. We describe a patient whose clinical and histopathological abnormalities are consistent with this diagnosis.

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Year:  2001        PMID: 11422044     DOI: 10.1046/j.1365-2133.2001.04235.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  4 in total

1.  Congenital hypotrichosis, eruptive milia, and palmoplantar pits: a case report with review of literature.

Authors:  Gk Tharini; M Subashini; S Anupama Roshan; D Prabhavathy; S Jayakumar
Journal:  Int J Trichology       Date:  2012-01

2.  [Genodermatoses with malignant skin tumors].

Authors:  L Hübinger; J Frank
Journal:  Hautarzt       Date:  2014-06       Impact factor: 0.751

Review 3.  Hereditary nonmelanoma skin cancer.

Authors:  Vasiliki Nikolaou; Alexander J Stratigos; Hensin Tsao
Journal:  Semin Cutan Med Surg       Date:  2012-12

4.  A case of bilateral scarring of the cheeks in a child.

Authors:  Yk Inchara; T Rajalakshmi; Mary Augustine
Journal:  J Cutan Aesthet Surg       Date:  2010-09
  4 in total

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