Mounira Meddeb

VP53.09: Alobar holoprosencephaly: a case report

Mounira Meddeb, M. Neifar, Fathi Mraihi, H. Ben Ahmed et autres

Holoprosencephaly is a rare brain abnormality resulting from an incomplete cleavage of the primitive prosencephalon of forebrain during early embryogenesis. It includes a series of rare complex and heterogenosis disorders. Facial anomalies are frequently associated, owing to the common origin of the …

Multiple myeloma with Auer-rod-like inclusions

Sarra Fekih Salem, Wijdène El Borgi, Fatma BenLakhal, Salma Kéfi et autres

Résumé Contexte. Au Sénégal, la réduction de la mortalité néonatale reste un défi. La prise en charge des infections néonatales demeure problématique et fortement focalisée sur la clinique. En effet, comme dans tous pays en voie de développement, la difficulté de l’acquisition …

Depth of Response to ≥VGPR at Completion of Induction Influences Outcome Post ASCT, on Behalf of the Tunisian Myeloma Study Group

Raoudha Mansouri, Rim El fatmi, Hèlà Ghédira, Faten Kallel et autres

Abstract Background: High dose Melphalan (HDM) and autologous stem cell transplantation (ASCT) is a standard care for Myeloma ≤ 65 years. Studies have demonstrated that depth of response prior to ASCT does not impact outcome post ASCT, e.g. solely depth of response …

Tunisie, fr (code pays fourni par la source)

Cytogenetic Assessment of Fanconi Anemia in Children With Aplastic Anemia in Tunisia

Faten Talmoudi, Lobna Kammoun, Nizar Benhalim, Lamia Torjemane et autres

BACKGROUND: Chromosome breakage hypersensitivity to alkylating agents is the gold standard test for Fanconi anemia (FA) diagnosis. The aim of the present study was to assess the proportion of FA cases among aplastic anemia (AA) in Tunisian pediatric patients. OBSERVATION: Investigation of …

Tunisie, gb, pl, fr (code pays fourni par la source)

Monosomy 10q26-qter and trisomy 11q13-qter as a result ofde novo unbalanced translocation

Faten Tinsa, Y. Chebbi, Mounira Meddeb, Dorra Bousnina et autres

Tunisie (code pays fourni par la source)

Multiple Congenital Anomalies/Mental Retardation Syndrome With Multiple Circumferential Skin Creases: A New Syndrome?

Faten Tinsa, Khaoula Aissa, Mounira Meddeb, Dorra Bousnina et autres

We describe a combination of multiple congenital anomalies, a severe psychomotor retardation and seizures in a 9-year-old Tunisian boy with circumferential ringed skin creases. He had symmetrical circumferential skin creases on arms, legs, and penis. Craniofacial anomalies included: an elongated face, tight …

Tunisie (code pays fourni par la source)

Identification and characterization of a new Leishmania major specific 3′nucleotidase/nuclease protein

Inès Lakhal-Naouar, Yosser Ben Achour-Chenik, Yvan Boublik, Mounira Meddeb et autres

Tunisie, fr (code pays fourni par la source)

MDM2 amplification in a primary alveolar rhabdomyosarcoma displaying a t(2;13)(q35;q14)

Mounira Meddeb, Arnaud Valent, G. Danglot, V.C. Nguyen et autres

This report describes a case of rhabdomyosarcoma associated with a 2;13 translocation and multiple double minute chromosomes. The origin of the amplified DNA was identified using comparative genomic hybridization, which pinpointed a unique spot at 12q13-->q14. Band 12q13 has been shown to …

fr (code pays fourni par la source)

Contents, Vol. 73, 1996

Nigel K. Spurr, Susan L. Naylor, Olga V. Zatsepina, Christian Schöfer et autres

Author Index, Vol. 73, 1996

Nigel K. Spurr, Susan L. Naylor, Olga V. Zatsepina, Christian Schöfer et autres

Characteristic Pattern of Chromosomal Imbalances in Posttransplantation Lymphoproliferative Disorders: Correlation with Histopathological Subcategories and EBV Status

Hélène Antoine Poirel, Alain Bernheim, Anouck Schneider, Mounira Meddeb et autres

BACKGROUND: Posttransplantation lymphoproliferative disorders (PTLDs) are a spectrum of lymphoid proliferations, occurring in immunosuppressed organ transplant recipients. They comprise early lesions, polymorphic (P-PTLD), monomorphic (M-PTLD), and Hodgkin/Hodgkin-like lymphoma PTLD (HL-PTLD) lesions. Most of them are associated with Epstein-Barr virus (EBV). Little is …

be, fr (code pays fourni par la source)

Distinct chromosomal abnormality pattern in primary liver cancer of non-B, non-C patients

Agnès Marchio, Pascal Pineau, Mounira Meddeb, Benoı̂t Terris et autres

fr (code pays fourni par la source)