Ichthyosis Follicularis in Two Girls: An Autosomal Dominant Disorder
- 1 December 1990
- journal article
- case report
- Published by Wiley in Pediatric Dermatology
- Vol. 7 (4) , 287-292
- https://doi.org/10.1111/j.1525-1470.1990.tb01027.x
Abstract
Ichthyosis follicularis (IF) is a rare disorder of keratinization that has been described primarily in males and proposed as a possible X-linked disorder. We report two black girls with nonscarring alopecia; photophobia; follicular hyperkeratoses; hyperkeratosis of the extensor aspects of the hands, knees, and elbows; fixed, erythematous, perineal plaques; and angular cheilitis who seem to fit the clinical criteria for IF. One girl also had gingival hypertrophy and a hearing deficit. One child's father had identical symptoms. We propose that these girls may have a variant of IF that is inherited as an autosomal dominant trait.Keywords
This publication has 3 references indexed in Scilit:
- Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomasArchives of Dermatology, 1987
- Ichthyosis follicularis with alopecia and photophobiaArchives of Dermatology, 1985
- The keratitis, ichthyosis, and deafness (KID) syndromeArchives of Dermatology, 1981