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6 results on '"Hachemane S"'

1. C028 - Est-ce que l’amantadine améliore la réponse virologique long terme de l’association Peg-Interféron-alpha2b/ribavirine chez les malades atteints d’hépatite chronique C n’ayant jamais reçu de traitement ? Étude prospective randomisée multicentrique en double aveugle : résultats préliminaires chez 200 malades

Author

Calay, V., primary, Hachemane, S., additional, Pageaux, G.P., additional, Bourlière, M., additional, Portal, I., additional, Mathurin, P., additional, Verdier, E., additional, Tran, A., additional, Bozonnat, C., additional, Daures, J.P., additional, Arpurt, J.P., additional, Goria, O., additional, Chassagne, P., additional, and Larrey, D., additional

Published
2005
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5. [Leiomyosarcoma and angiomyomatous hamartoma: An hasardous association?]

Author

Petitjean M, Kashi-Dakhil M, Hachemane S, Dakhil B, Zaimi R, and Bagan P

Subjects
Aged, 80 and over, Angiomyoma diagnostic imaging, Angiomyoma pathology, Femoral Vein diagnostic imaging, Femoral Vein surgery, Hamartoma diagnostic imaging, Hamartoma pathology, Humans, Leiomyosarcoma diagnostic imaging, Leiomyosarcoma pathology, Leiomyosarcoma surgery, Lymph Nodes pathology, Lymphatic Diseases diagnostic imaging, Lymphatic Diseases pathology, Male, Neoplasms, Multiple Primary diagnostic imaging, Neoplasms, Multiple Primary pathology, Positron-Emission Tomography, Pseudolymphoma complications, Pseudolymphoma diagnostic imaging, Pseudolymphoma pathology, Vascular Neoplasms diagnostic imaging, Vascular Neoplasms pathology, Vascular Neoplasms surgery, Angiomyoma complications, Femoral Vein pathology, Hamartoma complications, Leiomyosarcoma complications, Lymphatic Diseases complications, Lymphedema etiology, Vascular Neoplasms complications
Published
2020
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6. Disseminated Bacillus Calmette-Guérin Osteomyelitis in Twin Sisters Related to STAT1 Gene Deficiency.

Author

Boudjemaa S, Dainese L, Héritier S, Masserot C, Hachemane S, Casanova JL, Coulomb A, and Bustamante J

Subjects
Diseases in Twins diagnosis, Female, Genetic Diseases, Inborn complications, Genetic Diseases, Inborn genetics, Genetic Markers, Genetic Predisposition to Disease, Heterozygote, Humans, Infant, Mutation, Mycobacterium Infections diagnosis, Osteomyelitis diagnosis, STAT1 Transcription Factor deficiency, Diseases in Twins genetics, Genetic Diseases, Inborn diagnosis, Mycobacterium Infections genetics, Mycobacterium bovis isolation & purification, Osteomyelitis genetics, STAT1 Transcription Factor genetics
Abstract

Mendelian susceptibility to mycobacterial disease is a rare syndrome characterized by severe clinical infections usually caused by weakly virulent mycobacterial species such as Bacillus Calmette-Guérin vaccines and environmental nontuberculous mycobacteria or more virulent mycobacteria as mycobacterium tuberculosis. Since 1996, 9 genes including 7 autosomal ( STAT1, IFNGR1, IFNGR2, IL12B, IL12RB1, ISG15, and IRF8) and 2 X-linked genes ( NEMO and CYBB) have been identified. Allelic heterogeneity leaded to recognize about 18 genetic diseases with variable clinical phenotypes, but sharing a same physiological mechanism represented by a defect in human IL-12-dependant-INF-γ-mediated immunity. We report here a case of multifocal Bacillus Calmette-Guérin osteomyelitis in a context Mendelian susceptibility to mycobacterial disease mimicking a metastatic neuroblastoma in a child presenting with delayed growth. The investigation of her twin sister showed the same disease. A heterozygous mutation in exon 22 of STAT1 gene was found in both sisters, another sister and the father being healthy and heterozygous for the same mutation.

Published
2017
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