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.| Files | ||
| Issue | Vol 37, No 2 (1999) | |
| Section | Articles | |
| 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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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
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.
