Publications by authors named "Fadlouallah Maha"

Article Synopsis
  • - The study investigated the frequency of NOD2/CARD15 gene mutations in Moroccan patients with Crohn's disease, finding a 13.77% mutation rate compared to 6.53% in a control group of 107 patients.
  • - Three specific NOD2 gene variants (p.Arg702Trp, p.Gly908Arg, p.Leu1007fsins) were analyzed, revealing the most common mutation was p.Gly908Arg at 6.43% among patients.
  • - The research concluded that NOD2/CARD15 mutations are linked to more severe features of Crohn's disease, like ileocecal involvement and higher surgery and medication needs, even though the overall prevalence of mutations
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Ophthalmologic complications with interferon therapy are rare and usually reversible. The anterior ischemic optic neuropathy is an uncommon complication of interferon treatment. A case of irreversible anterior ischemic optic neuropathy complicating interferon therapy for chronic hepatitis C is reported.

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