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Article in English | MEDLINE | ID: mdl-21508573

ABSTRACT

Keratosis follicularis spinulosa decalvans (KFSD), is a rare follicular syndrome associated with widespread keratosis pilaris and progressive scarring alopecia. This genodermatoses often starts at infancy or early childhood with an X-linked mode of inheritance. Males are predominantly affected and females frequently show no disease or only a mild form. We describe this not so common entity of KFSD in a nine year old female child.


Subject(s)
Scalp/pathology , Biopsy , Cheek/pathology , Child , Eyebrows/pathology , Female , Genetic Diseases, X-Linked , Humans , Ichthyosis/pathology , Skin Diseases, Genetic
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