Literature DB >> 16409932

Ichthyosis follicularis with congenital atrichia, nail dystrophy and palmoplantar keratoderma. Variant of IFAP syndrome or a new entity?

Vandana Mehta Rai1, S D Shenoi.   

Abstract

A 23-year-old man was seen for dry, rough skin and alopecia present since birth. There was no history of impaired sweating, photophobia, or lacrimation. Examination revealed generalized cutaneous thorn-like projections with nonscarring alopecia, twenty-nail dystrophy, and palmoplantar keratoderma.

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Mesh：

Year:  2005        PMID： 16409932

Source DB:  PubMed          Journal:  Dermatol Online J        ISSN： 1087-2108


  3 in total

1.  Photoletter to the editor: A new variant of ichthyosis follicularis with alopecia and photophobia (IFAP) syndrome with coexisting psoriasiform lesions and palmoplantar keratoderma. IFAP-PPK syndrome?

Authors:  Mohammad Alshami; Mohammed A Bawazir; Ausama A Atwan
Journal:  J Dermatol Case Rep       Date:  2011-03-26

Review 2.  Trachyonychia and Twenty-Nail Dystrophy: A Comprehensive Review and Discussion of Diagnostic Accuracy.

Authors:  Audrey A Jacobsen; Antonella Tosti
Journal:  Skin Appendage Disord       Date:  2016-04-30

3.  Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome: A Case Report and Review of Cases Reported from India.

Authors:  Anupama Bains; Deepak Vedant; Anurag Verma; Abhishek Bhardwaj; Aasma Nalwa
Journal:  Indian Dermatol Online J       Date:  2019-11-01
  3 in total

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