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

Vandana Mehta Rai; S. D. Shenoi

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

Vandana Mehta Rai^*, S. D. Shenoi

^*Corresponding author for this work

Department of Dermatology, Venereology and Leprosy, Kasturba Medical College, Manipal

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

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.

Original language	English
Number of pages	1
Journal	Dermatology online journal [electronic resource].
Volume	11
Issue number	3
Publication status	Published - 01-12-2005

All Science Journal Classification (ASJC) codes

Dermatology

Cite this

@article{be0bd0f0c63d41c8ae27586fb36f8fc3,

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

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.",

author = "Rai, {Vandana Mehta} and Shenoi, {S. D.}",

year = "2005",

month = dec,

day = "1",

language = "English",

volume = "11",

journal = "Dermatology online journal [electronic resource].",

issn = "1087-2108",