Search Results - "Tajir, M."

Double isochromosome X, A rare cytogenetic variant of turner syndrome: A case report and a review of the literature by Zerrouki, K., Babakhouya, A., Tajir, M.

“…Turner Syndrome (TS) is a genetic disorder caused by total or partial loss of an X chromosome. The isochromosome X (i(X)) is a known variant of TS, however,…”
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Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene by Tajir, M, Lyahyai, J, Guaoua, S, El Alloussi, M, Sefiani, A

“…Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome is a rare genetic disease with an autosomal dominant transmission, characterized by several…”
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Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism by Twigg, S.R.F., Ousager, L.B., Miller, K.A., Zhou, Y., Elalaoui, S.C., Sefiani, A., Bak, G.S, Hove, H., Hansen, L.K., Fagerberg, C.R., Tajir, M., Wilkie, A.O.M.

“…Acromelic frontonasal dysostosis (AFND) is a distinctive and rare frontonasal malformation that presents in combination with brain and limb abnormalities. A…”
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Pregnancy revealing hereditary angioedema type III with factor XII mutation managed in a resource-limited setting with no C1-inhibitor concentrate availability: A case-report by Saddouk, H., Tajir, M., Saadi, H., Housni, B., Zerrouki, N., Zizi, N., Dikhaye, S.

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Acromelic frontonasal dysostosis and ZSWIM6 mutation: phenotypic spectrum and mosaicism: Acromelic frontonasal dysostosis and ZSWIM6 mutation by Twigg, S.R.F., Ousager, L.B., Miller, K.A., Zhou, Y., Elalaoui, S.C., Sefiani, A., Bak, G.S, Hove, H., Hansen, L.K., Fagerberg, C.R., Tajir, M., Wilkie, A.O.M.

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An inherited LMNA gene mutation in atypical Progeria syndrome by Doubaj, Yassamine, De Sandre‐Giovannoli, Annachiara, Vera, Esteves‐Vieira, Navarro, Claire Laure, Elalaoui, Siham Chafai, Tajir, Mariam, Lévy, Nicolas, Sefiani, Abdelaziz

“…Hutchinson–Gilford Progeria syndrome (HGPS) is a rare genetic disorder, characterized by several clinical features that begin in early childhood, recalling an…”
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Profil diagnostique et thérapeutique des dysgénésies gonadiques au CHU Mohammed VI Oujda by Elilie Mawa Ongoth, F., Farih, S., Tajir, M., Benhaddou, H., Latrech, H.

“…Les dysgénésies gonadiques (DG) constituent un pathologie caractérisée par un développement altéré des gonades (ovaire ou testicule) en rapport avec une…”
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Frequency of IL28B rs12979860 single-nucleotide polymorphism alleles in newborn infants and in patients with chronic hepatitis C in Morocco by Tajir, Mariam, Elmachad, Mustapha, Kabbaj, Nawal, Laarabi, Fatima Zahra, Barkat, Amina, Amrani, Naima, Sefiani, Abdelaziz

“…Epidemiological and experimental evidence support the role of host genetics in treatment response and viral clearance in chronic hepatitis C (CHC). Recently,…”
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Periodontal Health and Salivary Interleukin - 6 among Preterm Postpartum Women by Al-Obaidi , Wesal A, Tajer , Dhamiaa M

“…Background: Hormonal changes during pregnancy have been suggested to predispose women to gingivitis. Furthermore, advance periodontal infection in pregnant…”
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Dental Caries and Salivary Interleukin - 6 among Preterm Postpartum Women in Relation to Baby Birth Weight: Comparative Study by Al-Obaidi , Wesal A, Tajer , Dhamiaa M

“…Background: The physiologic, biochemical and anatomic changes that occur during pregnancy are extensive and may be systemic or local. However, most of these…”
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