Journal article
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity
Archives of Dermatological Research, Vol.304(2), pp.171-176
03/01/2012
DOI: 10.1007/s00403-011-1190-4
PMID: 22081045
Abstract
Xeroderma pigmentosum (XP) is a rare disorder characterized by a high skin sun-sensitivity predisposing to skin cancers at an early age. Among Tunisian XP patients with an intermediate skin phenotype, 92% presented neurological abnormalities related to XPA gene deficiency. Clinical variability of the XP-A phenotype is associated with a mutational heterogeneity. In the present study, two Tunisian families with severe dermatological and neurological XP phenotypes were investigated in order to determine clinical characteristics and genetic basis. Two Tunisian families with four XP affected children were examined in the Dermatology Department. Clinical features showed severe presentation of the disease. Coding regions of the XPA gene were analysed by direct sequencing. Results showed the presence of a novel mutation, p.E111X, in three patients belonging to the same family and presenting a very severe phenotype i.e. development of skin lesions and neurological signs before 1 year age. For the other patient, we identified a nonsense mutation, p.R207X, already identified in a Palestinian XP-A patient. Identification of novel causing mutations in Tunisian XP-A patients shows the genetic and mutational heterogeneity of the disease in Tunisia. Despite a relatively homogenous mutational spectrum, mutational heterogeneity for rare cases is observed because of the high rate of consanguinity.
Details
- Title: Subtitle
- Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity
- Creators
- O. Messaoud - Institut Pasteur de TunisM Ben Rekaya - Institut Pasteur de TunisH. Ouragini - Institut Pasteur de TunisS. Benfadhel - Institut Pasteur de TunisH. Azaiez - Institut Pasteur de TunisR. Kefi - Institut Pasteur de TunisN. Gouider-Khouja - National Institute of Neurology Mongi-Ben HamidaI. Mokhtar - Habib hospital ThameurA. Amouri - Institut Pasteur de TunisM. S. Boubaker - Institut Pasteur de TunisM. Zghal - Habib hospital ThameurS. Abdelhak - Institut Pasteur de Tunis
- Resource Type
- Journal article
- Publication Details
- Archives of Dermatological Research, Vol.304(2), pp.171-176
- Publisher
- Springer Verlag
- DOI
- 10.1007/s00403-011-1190-4
- PMID
- 22081045
- ISSN
- 0340-3696
- eISSN
- 1432-069X
- Language
- English
- Date published
- 03/01/2012
- Academic Unit
- Otolaryngology
- Record Identifier
- 9984383893902771
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