Literature DB >> 9873177

Peeling skin syndrome with hair changes.

B Mevorah1, E Orion, P de Viragh, R Bergman, A Gat, C Legume, D J Van Neste, S Brenner.   

Abstract

A 13-year-old boy with typical peeling skin syndrome (PSS) is described. The clinical picture corresponded to the inflammatory variant of PSS (type B). In addition, the patient had gross and microscopic hair anomalies such as trichorrhexis invaginata-like changes, irregular hair shaft torsions and moniliform hair shaft diameter reductions. The observed dysmorphic hair changes are discussed and interpreted as being an integral component of the dermatosis in this case. To the best of our knowledge, such hair anomalies have not yet been described in PSS.

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Year:  1998        PMID: 9873177     DOI: 10.1159/000018034

Source DB:  PubMed          Journal:  Dermatology        ISSN: 1018-8665            Impact factor:   5.366


  1 in total

1.  A novel pathogenic variant in the corneodesmosin gene causing generalized inflammatory peeling skin syndrome with marked eosinophilia and trichorrhexis invaginata.

Authors:  Helen Gordon; Patrick Yap; Kuang-Chih Hsiao; Michael Watson; Diana Purvis
Journal:  Pediatr Dermatol       Date:  2022-02-17       Impact factor: 1.997

  1 in total

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