Loose anagen hair syndrome in children of Upper Egypt
Summary Background Loose anagen hair (LAH) syndrome is a phenomenon in early childhood characterized by the presence of easily pluckable hair, where hair tufts can be pulled out easily and painlessly. Aims All reports in the English literature described mainly white patients with blond hair. We pr...
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Published in | Journal of cosmetic dermatology Vol. 8; no. 2; pp. 103 - 107 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.06.2009
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Subjects | |
Online Access | Get full text |
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Summary: | Summary
Background Loose anagen hair (LAH) syndrome is a phenomenon in early childhood characterized by the presence of easily pluckable hair, where hair tufts can be pulled out easily and painlessly.
Aims All reports in the English literature described mainly white patients with blond hair. We present the first report of LAH syndrome in dark‐skinned children of Upper Egypt.
Patients and methods Twenty‐eight children with LAH were diagnosed and examined from 1996 to 2007. The main complaints were patchy or diffuse alopecia and/or slow growth of hair. Clinical examination, hair pull test, trichogram, and scanning electron microscopy (SEM) were performed.
Results Children with LAH included 21 girls (75%) and seven boys (25%). Light microscopy of hair pull tests and trichograms disclosed a striking predominance of anagen hairs (90–100%) with misshapen hair bulbs and absent inner and outer root sheaths. SEM confirmed the misshapen anagen bulbs with ruffled appearance of cuticle and the longitudinal groove parallel to the long axis of the hair shaft. Most children improved spontaneously within few years, however, hair shed continued.
Conclusion LAH syndrome occurs in dark‐skinned children and could be under‐diagnosed. The condition is of cosmetic concern and does not affect the general health. |
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Bibliography: | istex:0909F1ED7861C6B0420245ABB74F6DBEE29133E1 ark:/67375/WNG-5M48VLP4-B ArticleID:JOCD434 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1473-2130 1473-2165 |
DOI: | 10.1111/j.1473-2165.2009.00434.x |