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Trichothiodystrophy in a Child with Occult Learning Disorder
Trichothiodystrophy (TTD) is an autosomal recessive condition characterized by brittle and sparse sulfur deficient hair. The disorder is due to a known genetic mutation in DNA nucleotide excision repair (NER) in up to 83% of cases. We describe a 13-month-old girl presenting with hair fragility and h...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746226/ https://www.ncbi.nlm.nih.gov/pubmed/23960396 http://dx.doi.org/10.4103/0974-7753.114717 |
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author | Oon, Hazel H Sze Chan, Agnes Wai See Lee, Joyce Siong Leow, Yung Hian Giam, Yoke Chin |
author_facet | Oon, Hazel H Sze Chan, Agnes Wai See Lee, Joyce Siong Leow, Yung Hian Giam, Yoke Chin |
author_sort | Oon, Hazel H |
collection | PubMed |
description | Trichothiodystrophy (TTD) is an autosomal recessive condition characterized by brittle and sparse sulfur deficient hair. The disorder is due to a known genetic mutation in DNA nucleotide excision repair (NER) in up to 83% of cases. We describe a 13-month-old girl presenting with hair fragility and hair loss since age 3 months, and discuss the overlap between TTD and other NER diseases. This case report highlights the importance of early diagnosis of occult learning disorder in young children with TTD and the need for early assessment and involvement of multidisciplinary team to target the child's educational needs. |
format | Online Article Text |
id | pubmed-3746226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-37462262013-08-19 Trichothiodystrophy in a Child with Occult Learning Disorder Oon, Hazel H Sze Chan, Agnes Wai See Lee, Joyce Siong Leow, Yung Hian Giam, Yoke Chin Int J Trichology Case Report Trichothiodystrophy (TTD) is an autosomal recessive condition characterized by brittle and sparse sulfur deficient hair. The disorder is due to a known genetic mutation in DNA nucleotide excision repair (NER) in up to 83% of cases. We describe a 13-month-old girl presenting with hair fragility and hair loss since age 3 months, and discuss the overlap between TTD and other NER diseases. This case report highlights the importance of early diagnosis of occult learning disorder in young children with TTD and the need for early assessment and involvement of multidisciplinary team to target the child's educational needs. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3746226/ /pubmed/23960396 http://dx.doi.org/10.4103/0974-7753.114717 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 Oon, Hazel H Sze Chan, Agnes Wai See Lee, Joyce Siong Leow, Yung Hian Giam, Yoke Chin Trichothiodystrophy in a Child with Occult Learning Disorder |
title | Trichothiodystrophy in a Child with Occult Learning Disorder |
title_full | Trichothiodystrophy in a Child with Occult Learning Disorder |
title_fullStr | Trichothiodystrophy in a Child with Occult Learning Disorder |
title_full_unstemmed | Trichothiodystrophy in a Child with Occult Learning Disorder |
title_short | Trichothiodystrophy in a Child with Occult Learning Disorder |
title_sort | trichothiodystrophy in a child with occult learning disorder |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746226/ https://www.ncbi.nlm.nih.gov/pubmed/23960396 http://dx.doi.org/10.4103/0974-7753.114717 |
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