Abstract
Abstract
In the modern medical literature, alopecia totalis has been reported as early as the 1940s. Childhood alopecia totalis is a heterogeneous disorder that occur in syndromic and non-syndromic forms and can have autoimmune, nutritional and genetic bases. Non-syndromic childhood alopecia totalis is generally has autoimmune bases. During the 1970s, authors reported the treatment of alopecia totalis with DNCB which is 1-chloro, 2, 4-dinitrobenzene and High-dose glucocorticoid. Early during the 1980s, oral photochemotherapy was used in the treatment of alopecia totalis without the occurrence of side effects. The aim of this paper is to present a case of childhood non-syndromic alopecia totalis and to review of the available evidence-based therapies.
Reference28 articles.
1. 1. Jaeger H. Alopecia decalvans, totalis, maligna, mit Nagelveränderungen und Zahnanomalien Dermatologica. 1945; 91:264.
2. 2. Miescher G. Trichomalacie der Haare bei Alopecia areata totalis. Dermatologica. 1946; 92:314-317.
3. 3. Schulze HD. Total alopecia in mother and daughter. Dermatol Wochenschr. 1966; 152:187-192.
4. 4. Senter TP, Jones KL, Sakati N, Nyhan. Atypical ichthyosiform erythroderma and congenital neurosensory deafness: A distinct syndrome. J Pediatr. 1978; 92:68-72.
5. 5. Hart ZH, Hoffman W, Winbaum E. Polyneuropathy, alopecia areata, and chronic lymphocytic thyroiditis. Neurology. 1979; 29:106-108.
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