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Familial Trichotillomania in Three Generations

Trichotillomania (TTM) is a type of impulse control disorder, characterized by recurrent pulling of hair. The etiology of TTM is complex, but a genetic contribution to this condition was advocated based on a limited number of reports on familial TTM. We report a 13-year-old male with history of foca...

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Autores principales: Ramot, Yuval, Maly, Alexander, Horev, Liran, Zlotogorski, Abraham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877480/
https://www.ncbi.nlm.nih.gov/pubmed/24403772
http://dx.doi.org/10.4103/0974-7753.122968
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author Ramot, Yuval
Maly, Alexander
Horev, Liran
Zlotogorski, Abraham
author_facet Ramot, Yuval
Maly, Alexander
Horev, Liran
Zlotogorski, Abraham
author_sort Ramot, Yuval
collection PubMed
description Trichotillomania (TTM) is a type of impulse control disorder, characterized by recurrent pulling of hair. The etiology of TTM is complex, but a genetic contribution to this condition was advocated based on a limited number of reports on familial TTM. We report a 13-year-old male with history of focal hair loss in the scalp. Examination showed a patchy area of hair loss, with several short broken hairs of varying lengths. Dermoscopy and pathology examinations were consistent with TTM. Upon further questioning, his father admitted repeated pulling of his beard. The paternal grandfather also suffers from severe hair pulling of his beard since puberty. To our knowledge, this is the first report of TTM in a 3 generation family. This report strengthens the possibility that TTM is a genetic disease, probably with a complex inheritance pattern. It also highlights the importance of appropriate family history taking when examining a TTM patient.
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spelling pubmed-38774802014-01-08 Familial Trichotillomania in Three Generations Ramot, Yuval Maly, Alexander Horev, Liran Zlotogorski, Abraham Int J Trichology Case Report Trichotillomania (TTM) is a type of impulse control disorder, characterized by recurrent pulling of hair. The etiology of TTM is complex, but a genetic contribution to this condition was advocated based on a limited number of reports on familial TTM. We report a 13-year-old male with history of focal hair loss in the scalp. Examination showed a patchy area of hair loss, with several short broken hairs of varying lengths. Dermoscopy and pathology examinations were consistent with TTM. Upon further questioning, his father admitted repeated pulling of his beard. The paternal grandfather also suffers from severe hair pulling of his beard since puberty. To our knowledge, this is the first report of TTM in a 3 generation family. This report strengthens the possibility that TTM is a genetic disease, probably with a complex inheritance pattern. It also highlights the importance of appropriate family history taking when examining a TTM patient. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3877480/ /pubmed/24403772 http://dx.doi.org/10.4103/0974-7753.122968 Text en Copyright: © International Journal of Trichology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Ramot, Yuval
Maly, Alexander
Horev, Liran
Zlotogorski, Abraham
Familial Trichotillomania in Three Generations
title Familial Trichotillomania in Three Generations
title_full Familial Trichotillomania in Three Generations
title_fullStr Familial Trichotillomania in Three Generations
title_full_unstemmed Familial Trichotillomania in Three Generations
title_short Familial Trichotillomania in Three Generations
title_sort familial trichotillomania in three generations
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877480/
https://www.ncbi.nlm.nih.gov/pubmed/24403772
http://dx.doi.org/10.4103/0974-7753.122968
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