Search Results - "Benfadhel, S."

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity by Messaoud, O., Ben Rekaya, M., Ouragini, H., Benfadhel, S., Azaiez, H., Kefi, R., Gouider-Khouja, N., Mokhtar, I., Amouri, A., Boubaker, M. S., Zghal, M., Abdelhak, S.

“…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…”
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The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosum by Messaoud, O, Ben Rekaya, M, Jerbi, M, Ouertani, I, Kefi, R, Laroussi, N, Bouyacoub, Y, Benfadhel, S, Yacoub-Youssef, H, Boubaker, S, Zghal, M, Mrad, R, Amouri, A, Abdelhak, S

“…Xeroderma pigmentosum (XP, OMIM 278700-278780) is one of the most severe genodermatoses and is relatively frequent in Tunisia. In the absence of any therapy…”
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