Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

Related collections

Author and article information

Contributors

Rahma Mkaouar: URI : https://loop.frontiersin.org/people/1416857/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role:

Zied Riahi: URI : https://loop.frontiersin.org/people/2664772/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role:

Jihene Marrakchi: URI : https://loop.frontiersin.org/people/2687360/overviewRole: Role: Role:

Nessrine Mezzi: URI : https://loop.frontiersin.org/people/2749133/overviewRole: Role: Role:

Lilia Romdhane: Role: Role: Role:

Maroua Boujemaa: URI : https://loop.frontiersin.org/people/956852/overviewRole: Role: Role:

Hamza Dallali: URI : https://loop.frontiersin.org/people/1277242/overviewRole: Role:

Marwa Sayeb: Role: Role:

Saida Lahbib: Role: Role:

Hajer Jaouadi: URI : https://loop.frontiersin.org/people/1124654/overviewRole: Role:

Hela Boudabbous: Role: Role: Role:

Lotfi Zekri: Role: Role: Role:

Mariem Chargui: Role: Role:

Olfa Messaoud: Role:

Meriem Elyounsi: Role:

Ichraf Kraoua: Role: Role:

Anissa Zaouak: URI : https://loop.frontiersin.org/people/2704955/overviewRole: Role: Role:

Ilhem Turki: URI : https://loop.frontiersin.org/people/2542141/overviewRole: Role: Role:

Mourad Mokni: Role: Role: Role:

Sophie Boucher: URI : https://loop.frontiersin.org/people/2687464/overviewRole: Role:

Christine Petit: URI : https://loop.frontiersin.org/people/846062/overviewRole: Role:

Fabrice Giraudet: URI : https://loop.frontiersin.org/people/477857/overviewRole: Role:

Chiraz Mbarek: Role: Role:

Ghazi Besbes: Role: Role: Role:

Soumeyya Halayem: URI : https://loop.frontiersin.org/people/930531/overviewRole: Role: Role:

Rim Zainine: Role: Role: Role:

Hamida Turki: Role: Role: Role:

Amel Tounsi: Role: Role: Role:

CRYSTEL Bonnet: URI : https://loop.frontiersin.org/people/2688890/overviewRole: Role: Role:

Ridha Mrad: Role: Role: Role: Role: Role: Role: Role: Role: Role:

Sonia Abdelhak: URI : https://loop.frontiersin.org/people/42850/overviewRole: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role: Role:

Mediha Trabelsi: Role: Role: Role: Role: Role: Role: Role: Role: Role:

Cherine Charfeddine: Role: Role: Role: Role: Role:

Journal

Journal ID (nlm-ta): Front Genet

Journal ID (iso-abbrev): Front Genet

Journal ID (publisher-id): Front. Genet.

Title: Frontiers in Genetics

Publisher: Frontiers Media S.A.

ISSN (Electronic): 1664-8021

Publication date (Electronic): 25 June 2024

Publication date Collection: 2024

Publication date PMC-release: 25 June 2024

Volume: 15

Electronic Location Identifier: 1437233

Affiliations

[1] ¹ Laboratory of Biomedical Genomics and Oncogenetics LR16IPT05 , Pasteur Institute in Tunis , University of Tunis El Manar , Tunis, Tunisia

[2] ² Department of Otorhinolaryngology , District Hospital of Menzel Bourguiba , Bizerte, Tunisia

[3] ³ Department of Biology , Faculty of Sciences of Bizerte , Université Tunis Carthage , Tunis, Tunisia

[4] ⁴ Genetic Typing Service , Institut Pasteur of Tunis , Tunis, Tunisia

[5] ⁵ Marseille Medical Genetics (MMG) U1251 , Aix Marseille Université , INSERM , Marseille, France

[6] ⁶ Department of Pediatrics , La Rabta Hospital , Tunis, Tunisia

[7] ⁷ Laboratory of Hereditary Diseases of the Metabolism Investigation and Patients Management , Faculty of Medicine in Tunis , University of Tunis El Manar , Tunis, Tunisia

[8] ⁸ Department of Epidemiology and Public Health , Directorate General of Military Health , Faculty of Medicine in Tunis , University of Tunis El Manar , Tunis, Tunisia

[9] ⁹ ICHARA Association (International Research Institute on Sign Language) , Tunis, Tunisia

[10] ¹⁰ Department of Congenital and Hereditary Diseases , Charles Nicolle Hospital in Tunis , Tunis, Tunisia

[11] ¹¹ LR99ES10 Laboratory of Human Genetics , Faculty of Medicine in Tunis , University of Tunis El Manar , Tunis, Tunisia

[12] ¹² Child and Adolescent Neurology Department of Neurology , National Institute of Neurology , Tunis, Tunisia

[13] ¹³ LR18SP04 Department of Child Neurology , National Institute Mongi Ben Hmida of Neurology in Tunis. University of Tunis El Manar , Tunis, Tunisia

[14] ¹⁴ Department of Dermatology , Habib Thameur Hospital , Research Unit Genodermatoses and Cancers LR12SP03 , Tunis, Tunisia

[15] ¹⁵ Service de dermatologie , Hôpital La Rabta , Unité de recherche UR 12SP07 , Hôpital La Rabta , Tunis, Tunisia

[16] ¹⁶ Service d’ORL et chirurgie cervico-faciale , CHU d’Angers , Angers, France

[17] ¹⁷ Equipe Mitolab , Institut Mitovasc , CNRS UMR6015 , UMR Inserm 1083 , Université d’Angers , Angers, France

[18] ¹⁸ Institut Pasteur , Université Paris Cité , Inserm UA06 , Institut de l’Audition , Paris, France

[19] ¹⁹ Collège de France , Paris, France

[20] ²⁰ Unité Mixte de Recherche (UMR) 1107 , INSERM , Clermont-Ferrand, France

[21] ²¹ Centre Auditif SoluSons , Clermont-Ferrand, France

[22] ²² Service de Génétique Médicale , CHU de Clermont-Ferrand , Clermont-Ferrand, France

[23] ²³ ENT Department , Habib Thameur Hospital , Tunis, Tunisia

[24] ²⁴ Department of Otorhinolaryngology and Maxillofacial Surgery—La Rabta Hospital in Tunis , Tunis, Tunisia

[25] ²⁵ Service de pédopsychiatrie , Hôpital Razi , Faculté de Médecine de Tunis , Université Tunis el Manar , Tunis, Tunisia

[26] ²⁶ Dermatology Department Hedi Chaker University Hospital , Sfax University Sfax Tunisia , Tunis, Tunisia

[27] ²⁷ CNSS Polyclinic , Bizerte, Tunisia

[28] ²⁸ Université de la Manouba , Institut de Biotechnologie de Sidi–Thabet , Ariana, Tunisia

Author notes

Edited and reviewed by: Ferran Casals, University of Barcelona, Spain

*Correspondence: Rahma Mkaouar, rahma.mkaouar@ 123456fst.utm.tn

Article

Publisher ID: 1437233

DOI: 10.3389/fgene.2024.1437233

PMC ID: 11231432

PubMed ID: 38983270

SO-VID: 23a3cd50-c9dc-41d0-ac3e-b720c88fce8d

Copyright © Copyright © 2024 Mkaouar, Riahi, Marrakchi, Mezzi, Romdhane, Boujemaa, Dallali, Sayeb, Lahbib, Jaouadi, Boudabbous, Zekri, Chargui, Messaoud, Elyounsi, Kraoua, Zaouak, Turki, Mokni, Boucher, Petit, Giraudet, Mbarek, Besbes, Halayem, Zainine, Turki, Tounsi, Bonnet, Mrad, Abdelhak, Trabelsi and Charfeddine.

License:

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

History

Date received : 23 May 2024

Date accepted : 27 May 2024

Custom metadata

section-at-acceptance Genetics of Common and Rare Diseases

ScienceOpen disciplines: Genetics

Keywords: syndromic deafness (sd),spectrum of sds,next-generation sequencing (ngs),early detection,under-diagnosis,tunisia

Data availability:

ScienceOpen disciplines: Genetics

Keywords: syndromic deafness (sd), spectrum of sds, next-generation sequencing (ngs), early detection, under-diagnosis, tunisia

Comments

Comment on this article

scite_