Original Article

KERATOSIS FOLLICULARIS SPINULOSA DECALVANS: REPORT OF A CASE AND LITERATURE REVIEW

Abstract

Keratosis follicularis spinulosa decalvans (KFSD) represents a rare, probably X-linked recessive genodermatosis, characterized by keratosis pilaris of face, trunk and extremities, followed by atrophy, cicatricial alopecia of the scalp, eyebrows and eyelashes, photophobia and corneal abnormalities. We report a rare case of KFSD and review the literature.
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IssueVol 37, No 2 (1999) QRcode
SectionOriginal Article(s)
Keywords
Keratosis pilaris atrophicans keratosis follicularis spinulosa decalvans ulerythema ophryogenes atrophoderma vermiculara ichthyosis follicularis with photophobia and alopecia ichthyosis deafness (KID) syndrome
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How to Cite
1.
P. Mansouri., M. R. Mortazavi Z. Saraii Naragki. KERATOSIS FOLLICULARIS SPINULOSA DECALVANS: REPORT OF A CASE AND LITERATURE REVIEW. Acta Med Iran. 1;37(2):123-127.