Skip to Main content Skip to Navigation
Journal articles

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.

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.
Document type :
Journal articles
Complete list of metadatas

Cited literature [20 references]  Display  Hide  Download

https://hal-riip.archives-ouvertes.fr/pasteur-00734400
Contributor : Institut Pasteur Tunis <>
Submitted on : Friday, September 21, 2012 - 4:39:18 PM
Last modification on : Monday, October 8, 2018 - 5:44:08 PM
Long-term archiving on: : Friday, December 16, 2016 - 3:16:01 PM

File

 Restricted access
To satisfy the distribution rights of the publisher, the document is embargoed until : jamais

Please log in to resquest access to the document

Identifiers

Collections

Citation

O. Messaoud, M Ben Rekaya, H. Ouragini, S. Benfadhel, H. Azaiez, et al.. Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.. Archives of Dermatological Research, Springer Verlag, 2012, 304 (2), pp.171-6. ⟨10.1007/s00403-011-1190-4⟩. ⟨pasteur-00734400⟩

Share

Metrics

Record views

127