Trichothiodystrophy group A: A first Japanese patient with a novel homozygous nonsense mutation in the GTF2H5 gene. Issue 8 (2nd July 2014)
- Record Type:
- Journal Article
- Title:
- Trichothiodystrophy group A: A first Japanese patient with a novel homozygous nonsense mutation in the GTF2H5 gene. Issue 8 (2nd July 2014)
- Main Title:
- Trichothiodystrophy group A: A first Japanese patient with a novel homozygous nonsense mutation in the GTF2H5 gene
- Authors:
- Moriwaki, Shinichi
Saruwatari, Hiroshi
Kanzaki, Tamotsu
Kanekura, Takuro
Minoshima, Shinsei - Abstract:
- <abstract abstract-type="main" id="jde12549-abs-0001"> <title>Abstract</title> <p>Trichothiodystrophy group A (TTD‐A) is one of the three types of photosensitive TTD and is a very rare genodermatosis with deficient post‐ultraviolet (UV) DNA repair. We herein describe the first Japanese case with a novel mutation in the <italic>GTF2H5</italic> gene responsible for TTD‐A. A 5‐year‐old male, born as a collodion baby from healthy non‐consanguineous parents, exhibited sun sensitivity, brittle hair, ichthyosis, cataracts and mental/physical retardation. He demonstrated neither neurological abnormalities nor pigmentary changes following sun exposure. The patient's primary fibroblasts were hypersensitive to killing by UV (<italic>D</italic><sub>0</sub> = 1.5 J/m<sup>2</sup>), and the post‐UV unscheduled DNA synthesis was 13% of normal. A host cell reactivation complementation analysis showed a decreased DNA capacity without recovery after transfecting any xeroderma pigmentosum genes. We identified a novel homozygous mutation (c.166G&gt;T) in the coding region of the <italic>GTF2H5</italic> gene that resulted in a predicted amino acid change: p.E55X. Thus far, only one Japanese case of TTD with a mutation of the <italic>XPD</italic> gene had been reported. The present case is the first of TTD‐A and the second case of TTD in Japan, suggesting that it is necessary to differentiate TTD from other photosensitive disorders, although the incidence of TTD is very low in Japan compared to<abstract abstract-type="main" id="jde12549-abs-0001"> <title>Abstract</title> <p>Trichothiodystrophy group A (TTD‐A) is one of the three types of photosensitive TTD and is a very rare genodermatosis with deficient post‐ultraviolet (UV) DNA repair. We herein describe the first Japanese case with a novel mutation in the <italic>GTF2H5</italic> gene responsible for TTD‐A. A 5‐year‐old male, born as a collodion baby from healthy non‐consanguineous parents, exhibited sun sensitivity, brittle hair, ichthyosis, cataracts and mental/physical retardation. He demonstrated neither neurological abnormalities nor pigmentary changes following sun exposure. The patient's primary fibroblasts were hypersensitive to killing by UV (<italic>D</italic><sub>0</sub> = 1.5 J/m<sup>2</sup>), and the post‐UV unscheduled DNA synthesis was 13% of normal. A host cell reactivation complementation analysis showed a decreased DNA capacity without recovery after transfecting any xeroderma pigmentosum genes. We identified a novel homozygous mutation (c.166G&gt;T) in the coding region of the <italic>GTF2H5</italic> gene that resulted in a predicted amino acid change: p.E55X. Thus far, only one Japanese case of TTD with a mutation of the <italic>XPD</italic> gene had been reported. The present case is the first of TTD‐A and the second case of TTD in Japan, suggesting that it is necessary to differentiate TTD from other photosensitive disorders, although the incidence of TTD is very low in Japan compared to that observed in Western countries.</p> </abstract> … (more)
- Is Part Of:
- Journal of dermatology. Volume 41:Issue 8(2014)
- Journal:
- Journal of dermatology
- Issue:
- Volume 41:Issue 8(2014)
- Issue Display:
- Volume 41, Issue 8 (2014)
- Year:
- 2014
- Volume:
- 41
- Issue:
- 8
- Issue Sort Value:
- 2014-0041-0008-0000
- Page Start:
- 705
- Page End:
- 708
- Publication Date:
- 2014-07-02
- Subjects:
- Dermatology -- Periodicals
Dermatology -- Japan -- Periodicals
Skin -- Diseases -- Periodicals
616.5005 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1346-8138 ↗
http://www.blackwell-synergy.com/loi/jde ↗
http://www.dermatol.or.jp/Journal/JD/index-e.html ↗
http://www.dermatol.or.jp/Journal/JD/index.html ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1346-8138.12549 ↗
- Languages:
- English
- ISSNs:
- 0385-2407
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4968.770000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4111.xml