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12. Abstract #1305594: Real-Life Effectiveness and Care Patterns of Diabetes Management in Eastern Europe, Middle East, and Africa (RECAP-DM EEMEA STUDY)

Author

Sieberhagen, Adrian, primary, Tayeb, Khalid, additional, Al Sifri, Saud, additional, Shestakova, Marina, additional, Amod, Aslam, additional, Zakaria, Ebtesam, additional, Azzouz, Malha, additional, Assaad-Khalil, Samir, additional, Harb, Salah, additional, Malek, Rachid, additional, Al Arouj, Monira, additional, Bennakhi, Abdullah, additional, Olegovna, Ten, additional, Voss, Bernd, additional, Loulou, Maysoon, additional, and Myrga, Zankel, additional

Published
2022
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19. Vitamin D deficiency and primary hyperparathyroidism

Author

Aicha Bouzid, Azzouz Malha, and Djamila Meskine

Subjects
medicine.medical_specialty, Endocrinology, business.industry, Internal medicine, medicine, medicine.disease, business, vitamin D deficiency, Primary hyperparathyroidism
Published
2021

20. Male osteoporosis

Author

Aicha Bouzid, Djamila Meskine, and Azzouz malha

Published
2021

21. Topographic diagnosis of primary hyperparathyroidism

Author

Azzouz Malha, Aicha Bouzid, and Djamila Meskine

Subjects
medicine.medical_specialty, business.industry, medicine, Radiology, medicine.disease, business, Primary hyperparathyroidism
Published
2021

23. Obesity in Bardet–Biedl syndrome

Author

Ztaitou Khaoula, Djamila Meskine, Aicha Bouzid, and Azzouz Malha

Subjects
Pediatrics, medicine.medical_specialty, business.industry, medicine, business, medicine.disease, Obesity
Published
2021

25. Maturity-Onset Diabetes of the Young Identified Among Algerian Probands with Early-Onset Diabetes

Author

Bouldjennet, Faiza, Gjesing, Anette P, Azzouz, Malha, Abderrahman, Samir Ait, El Guecier, Amina, Ali, Said, Oudjit, Brahim, Mennadi-Lacete, Farida, Yargui, Lyèce, Boudiba, Aissa, Chibane, Ahcène, Touil-Boukoffa, Chafia, Hansen, Torben, and Raache, Rachida

Subjects
endocrine system, HUMAN GLUCOKINASE GENE, GCK-MODY, type 1 diabetes, MUTATIONS, CHILDREN, VARIANTS, DIAGNOSIS, FAMILIES, PREVALENCE, MELLITUS, CLINICAL CHARACTERISTICS, MODY, monogenic diabetes, early-onset, genes, Targets and Therapy [Diabetes, Metabolic Syndrome and Obesity], Original Research
Abstract

Faiza Bouldjennet,1,* Anette P Gjesing,2,* Malha Azzouz,3 Samir Ait Abderrahman,4 Amina El Guecier,5 Said Ali,6 Brahim Oudjit,4 Farida Mennadi-Lacete,7 Lyèce Yargui,6 Aissa Boudiba,3 Ahcène Chibane,5 Chafia Touil-Boukoffa,1 Torben Hansen,2 Rachida Raache1 1Laboratory of Cellular and Molecular Biology, Cytokine and NO Synthase Team, University of Science and Technology, Houari Boumediene (USTHB), Algiers, Algeria; 2The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark; 3Diabetology Department of Mustapha Pacha Hospital, Algiers, Algeria; 4Diabetology Department of Mohamed Seghir Nekkache Hospital, Algiers, Algeria; 5Internal Medicine Department of Djillali Bounaâma Hospital, Algiers, Algeria; 6Laboratory of Biochemistry, Mustapha Pacha, Algiers, Algeria; 7Pediatric Department of Parnet Hospital, Algiers, Algeria*These authors contributed equally to this workCorrespondence: Anette P Gjesing; Rachida Raache Email anette.gjesing@sund.ku.dk; raache_ipa@yahoo.frAim: To investigate the prevalence of variants within selected maturity-onset diabetes of the young (MODY)-genes among Algerian patients initially diagnosed with type 1 diabetes (T1D) or type 2 diabetes (T2D), yet presenting with a MODY-like phenotype.Methods: Eight unrelated patients with early-onset diabetes (before 30 years) and six relatives with diabetes were examined by targeted re-sequencing for variants in genes known to be involved in MODY (HNF1A, GCK, HNF4A, HNF1B, INS, ABCC8, KCNJ1). Clinical data for probands were retrieved from hospital records.Results: A total of 12 variants were identified, of which three were classified as pathogenic and one as a variant of uncertain clinical significance (VUS). Two of the pathogenic variants were found in GCK (p.Gly261Arg and p.Met210Lys, respectively) in one proband each and the remaining pathogenic variant was found in HNF1B (p.Gly76Cys) in a proband also carrying the VUS in HNF1A (p.Thr156Met).Conclusion: Variants in known MODY-genes can be the cause of early-onset diabetes in Algerians diagnosed with T1D or T2D among patients presenting with a MODY-like phenotype; thus, genetic screening should be considered.Keywords: MODY, type 1 diabetes, early-onset, monogenic diabetes, genes

Published
2020

26. Maturity-Onset Diabetes of the Young Identified Among Algerian Probands with Early-Onset Diabetes

Author

Bouldjennet,Faiza, Gjesing,Anette P, Azzouz,Malha, Abderrahman,Samir Ait, El Guecier,Amina, Ali,Said, Oudjit,Brahim, Mennadi-Lacete,Farida, Yargui,Lyèce, Boudiba,Aissa, Chibane,Ahcène, Touil-Boukoffa,Chafia, Hansen,Torben, Raache,Rachida, Bouldjennet,Faiza, Gjesing,Anette P, Azzouz,Malha, Abderrahman,Samir Ait, El Guecier,Amina, Ali,Said, Oudjit,Brahim, Mennadi-Lacete,Farida, Yargui,Lyèce, Boudiba,Aissa, Chibane,Ahcène, Touil-Boukoffa,Chafia, Hansen,Torben, and Raache,Rachida

Abstract

Faiza Bouldjennet,1,* Anette P Gjesing,2,* Malha Azzouz,3 Samir Ait Abderrahman,4 Amina El Guecier,5 Said Ali,6 Brahim Oudjit,4 Farida Mennadi-Lacete,7 Lyèce Yargui,6 Aissa Boudiba,3 Ahcène Chibane,5 Chafia Touil-Boukoffa,1 Torben Hansen,2 Rachida Raache1 1Laboratory of Cellular and Molecular Biology, Cytokine and NO Synthase Team, University of Science and Technology, Houari Boumediene (USTHB), Algiers, Algeria; 2The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark; 3Diabetology Department of Mustapha Pacha Hospital, Algiers, Algeria; 4Diabetology Department of Mohamed Seghir Nekkache Hospital, Algiers, Algeria; 5Internal Medicine Department of Djillali Bounaâma Hospital, Algiers, Algeria; 6Laboratory of Biochemistry, Mustapha Pacha, Algiers, Algeria; 7Pediatric Department of Parnet Hospital, Algiers, Algeria*These authors contributed equally to this workCorrespondence: Anette P Gjesing; Rachida Raache Email anette.gjesing@sund.ku.dk; raache_ipa@yahoo.frAim: To investigate the prevalence of variants within selected maturity-onset diabetes of the young (MODY)-genes among Algerian patients initially diagnosed with type 1 diabetes (T1D) or type 2 diabetes (T2D), yet presenting with a MODY-like phenotype.Methods: Eight unrelated patients with early-onset diabetes (before 30 years) and six relatives with diabetes were examined by targeted re-sequencing for variants in genes known to be involved in MODY (HNF1A, GCK, HNF4A, HNF1B, INS, ABCC8, KCNJ1). Clinical data for probands were retrieved from hospital records.Results: A total of 12 variants were identified, of which three were classified as pathogenic and one as a variant of uncertain clinical significance (VUS). Two of the pathogenic variants were found in GCK (p.Gly261Arg and p.Met210Lys, respectively) in one proband each and the remaining pathogenic variant was found in HNF1B (p.Gly76Cys) in a proba

Published
2020

27. Maturity-Onset Diabetes of the Young Identified Among Algerian Probands with Early-Onset Diabetes

Author

Bouldjennet, Faiza, primary, Gjesing, Anette P, additional, Azzouz, Malha, additional, Abderrahman, Samir Ait, additional, El Guecier, Amina, additional, Ali, Said, additional, Oudjit, Brahim, additional, Mennadi-Lacete, Farida, additional, Yargui, Lyèce, additional, Boudiba, Aissa, additional, Chibane, Ahcène, additional, Touil-Boukoffa, Chafia, additional, Hansen, Torben, additional, and Raache, Rachida, additional

Published
2020
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29. Metabolic Imbalance and Vitamin D Deficiency in Type 1 Diabetes in the Algerian Population

Author

Mihoubi, Esma, primary, Raache, Rachida, additional, Amroun, Habiba, additional, Azzouz, Malha, additional, Galleze, Assia, additional, Zaabat, Nesrine, additional, Aissou, Abdelghani, additional, Ferhat, Amina, additional, Guettaf-Sadi, Hassiba, additional, Boutemeur, Amel, additional, Aoudia, Zoulikha, additional, Boudiba, Aissa, additional, Touil-Boukoffa, Chafia, additional, Abbadi, Mohamed C., additional, and Attal, Nabila, additional

Published
2019
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30. Human Leukocyte Antigens (HLA) Genes Association in Type 1 Diabetic Nephropathy

Author

Mihoubi, Esma, primary, Amroun, Habiba, additional, Raache, Rachida, additional, Bouldjennet, Faiza, additional, Meçabih, Fethi, additional, Azzouz, Malha, additional, Boudiba, Aissa, additional, Mahgoun, Souad, additional, Akachouche, Malika, additional, Salhi, Nawel, additional, Touil-Boukoffa, Chafia, additional, Abbadi, Mohamed C., additional, and Attal, Nabila, additional

Published
2019
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35. Association of major histocompatibility complex class 1 chain-related gene a dimorphism with type 1 diabetes and latent autoimmune diabetes in adults in the Algerian population

Author

UCL - SSS/IREC - Institut de recherche expérimentale et clinique, UCL - (SLuc) Service de biologie hématologique, Raache, Rachida, Belanteur, Khadidja, Amroun, Habiba, Benyahia, Amel, Heniche, Amel, Azzouz, Malha, Mimouni, Safia, Gervais, Thibaut, Latinne, Dominique, Boudiba, Aissa, Attal, Nabila, Abbadi, Mohamed Cherif, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, UCL - (SLuc) Service de biologie hématologique, Raache, Rachida, Belanteur, Khadidja, Amroun, Habiba, Benyahia, Amel, Heniche, Amel, Azzouz, Malha, Mimouni, Safia, Gervais, Thibaut, Latinne, Dominique, Boudiba, Aissa, Attal, Nabila, and Abbadi, Mohamed Cherif

Abstract

Major histocompatibility complex class I chain-related gene A (MICA-129) dimorphism was investigated in 73 autoimmune diabetes patients (type 1 diabetes and latent autoimmune diabetes in adults) and 75 controls from Algeria. Only MICA-129 Val allele and MICA-129 Val/Val genotype frequencies were higher among patients than in the control group. Statistical analysis of the estimated extended HLA-DR-DQ-MICA haplotypes shown that individual effects of MICA alleles on HLA-DQ2-DR3-MICA-129 Val/Val and HLA-DQ8-DR4-MICA-129 Val/Val haplotypes were significantly higher in patients than in the control groups. These preliminary data might suggest a relevant role of MICA-129 Val/Val single nucleotide polymorphism (weak/weak binders of NKG2D receptor) in the pathogenesis of T1D and LADA.

Published
2012

36. Association of Major Histocompatibility Complex Class 1 Chain-Related Gene A Dimorphism with Type 1 Diabetes and Latent Autoimmune Diabetes in Adults in the Algerian Population

Author

Raache, Rachida, primary, Belanteur, Khadidja, additional, Amroun, Habiba, additional, Benyahia, Amel, additional, Heniche, Amel, additional, Azzouz, Malha, additional, Mimouni, Safia, additional, Gervais, Thibaud, additional, Latinne, Dominique, additional, Boudiba, Aissa, additional, Attal, Nabila, additional, and Abbadi, Mohamed Cherif, additional

Published
2012
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