Genetic heterogeneity of prelingual severe to profound hearing impairment in patients from North African countries and Jordan

被引：0

作者：

Riahi, Zied ^{[1
]}

Boucher, Sophie ^{[2
]}

Tai, Fabienne Wong Jun ^{[1
]}

Estivalet, Amrit ^{[1
]}

Niasme-Grare, Magali ^{[3
]}

Bouyacoub, Yosra ^{[1
]}

Abdi, Samia ^{[4
]}

Dahmani, Malika ^{[5
]}

Talbi, Sonia ^{[5
]}

Mkouar, Rhama ^{[6
]}

Amalou, Ghita ^{[7
]}

Elrharchi, Soukaina ^{[7
]}

Mustafa, Mirna ^{[8
]}

Salame, Malak ^{[9
]}

Moctar, Ely Cheikh ^{[9
]}

Hadrami, Mouna ^{[9
]}

Charfeddine, Cherine ^{[6
]}

Jihene, Marrakchi ^{[10
]}

Zainine, Rim ^{[10
]}

Chahed, Houda ^{[10
]}

Ghazi, Besbes ^{[10
]}

Trabelsi, Mediha ^{[11
]}

Mrad, Ridha ^{[11
]}

Kraoua, Ichraf ^{[12
]}

Turki, Ilhem ^{[12
]}

Houmeida, Ahmed ^{[9
]}

Barakat, Abdelhamid ^{[7
]}

Ammar-Khodja, Fatima ^{[5
]}

Zenati, Akila ^{[13
]}

Makrelouf, Mohamed ^{[13
]}

Abdelhak, Sonia ^{[6
]}

Petit, Christine ^{[1
]}

Bonnet, Crystel ^{[1
]}

机构：

[1] Inst Pasteur, Inst Audit, INSERM, Paris, France

[2] Ctr Hosp Univ CHU Angers, Fac Med, Serv ORL, Angers, France

[3] Hop Enfants Armand Trousseau, AP HP, Serv Biochim & Biol Mol, Paris, France

[4] Univ Alger 1, Univ Saad Dahleb, Fac Med,Lab Cent Biol,CHU Frantz Fanon,Fac Med, Serv Biol,CHU Bab El Oued,Lab Biochim Genet, Algiers, Algeria

[5] Univ Sci & Technol Houari Boumed USTHB, Fac Sci Biol, Lab Biol Cellulaire & Mol, Equipe Genet, Algiers, Algeria

[6] Inst Pasteur Tunis, Biomed Genom & Oncogenet Lab, LR16IPT05, Tunis, Tunisia

[7] Inst Pasteur Maroc, Human Mol Genet Lab, Casablanca, Morocco

[8] Univ Sheffield, Dept Biomed Sci, Sheffield, England

[9] Univ Sci Technol & Med USTM, Unite Rech Biomarqueurs Populat Mauritanie, Nouakchott, Mauritania

[10] Hop Rabta, Otorhinolaryngol Dis, Tunis, Tunisia

[11] Hop Charles Nicolle, Congenital & Hereditary Dis, Tunis, Tunisia

[12] Inst Natl Neurol, Tunis, Tunisia

[13] Univ Alger 1, Serv Biol, Lab Biochim Genet, CHU Bab el Oued, Algiers, Algeria

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

P03.005.B

引用

页码：366 / 367

页数：2

共 17 条

[1] Effects of Early Identification and Intervention on Language Development in Japanese Children With Prelingual Severe to Profound Hearing Impairment
Kasai, Norio
Fukushima, Kunihiro
Omori, Kana
Sugaya, Akiko
Ojima, Toshiyuki
[J]. ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 2012, 121 (04): : 16 - 20
[2] Patients with severe-to-profound hearing impairment and simultaneous severe vision impairment: a quality-of-life study
Turunen-Taheri, Satu
Skagerstrand, Asa
Hellstrom, Sten
Carlsson, Per-Inge
[J]. ACTA OTO-LARYNGOLOGICA, 2017, 137 (03) : 279 - 285
[3] Rehabilitation of adult patients with severe-to-profound hearing impairment - why not cochlear implants?
Turunen-Taheri, Satu Kristiina
Eden, Margareta
Hellstrom, S.
Carlsson, Per-Inge
[J]. ACTA OTO-LARYNGOLOGICA, 2019, 139 (07) : 604 - 611
[4] Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaia province
Talbi, Sonia
Bonnet, Crystel
Riahi, Zied
Boudjenah, Farid
Dahmani, Malika
Hardelin, Jean-Pierre
Tai, Fabienne Wong Jun
Louha, Malek
Ammar-Khodja, Fatima
Petit, Christine
[J]. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2018, 112 : 1 - 5
[5] Molecular diagnosis of hereditary hearing impairment by high throughput sequencing of targeted exome in patients from Jordan and North Africa
Riahi, Z.
Bonnet, C.
Bouyacoub, Y.
Elamraoui, A.
Hardelin, J.
Ktaifi, C.
Sayeb, M.
Marrakchi, J.
Besbes, G.
Trabelsi, M.
Mrad, R.
Bakchane, A.
Charoute, H.
Snoussi, K.
Barakat, A.
Bahlouli, A.
Abdi, S.
Makrelouf, M.
Zenati, A.
Dahmani, M.
Talbi, S.
Khodja, F. Ammar
Elhachimie, H.
Houmeida, A.
Moctar, E. Mohamed
Hashim, M. Medlej
Abdelhak, S.
Petit, C.
[J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 177 - 177
[6] Hearing impairment: from extreme genetic heterogeneity for monogenic forms to complex forms
van Camp, Guy
[J]. JOURNAL OF MEDICAL GENETICS, 2006, 43 : S26 - S26
[7] Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis
Alerasool, Masoome
Eslahi, Atieh
Vona, Barbara
Kahaei, Mir Salar
Mojaver, Nasrin Kaseb
Rajati, Mohsen
Pasdar, Alireza
Ghasemi, Mohammad Mehdi
Saburi, Ehsan
Ardehaie, Reza Mousavi
Aval, Majid Hadadi
Tale, Mohammad Reza
Nourizadeh, Navid
Afzalzadeh, Mohammad Reza
Niknezhad, Hamid Tayarani
Mojarrad, Majid
[J]. CLINICAL GENETICS, 2024,
[8] NADf Chip, a Two-Color Microarray for Simultaneous Screening of Multigene Mutations Associated with Hearing Impairment in North African Mediterranean Countries
Chakchouk, Imen
Ben Said, Mariem
Jbeli, Fida
Benmarzoug, Riadh
Loukil, Salma
Smeti, Ibtihel
Chakroun, Amine
Gibriel, Abdullah Ahmed
Ghorbel, Abdelmonem
Hadjkacem, Hassen
Masmoudi, Saber
[J]. JOURNAL OF MOLECULAR DIAGNOSTICS, 2015, 17 (02): : 155 - 161
[9] PREVALENCE OF GENETIC MARKERS OF OXIDATIVE STRESS IN PATIENTS WITH SEVERE HEMOPHILIA FROM NORTH-WESTERN RUSSIA
Kapustin, S.
Aleksanyan, L.
Rybakova, L.
Kargin, V.
Burakov, V.
Svitina, S.
Titov, A.
Soldatenkov, V.
Chechetkin, A.
[J]. HAEMATOLOGICA, 2017, 102 : 96 - 97
[10] Quantifying the Diagnostic Pathway for Patients with Cognitive Impairment: Real-World Data from Seven European and North American Countries
Ritchie, Craig W.
Black, Christopher M.
Khandker, Rezaul K.
Wood, Robert
Jones, Eddie
Hu, Xiaohan
Ambegaonkar, Baishali M.
[J]. JOURNAL OF ALZHEIMERS DISEASE, 2018, 62 (01) : 457 - 466

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