Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic etiologies. In Tunisia, HI underdiagnosis prevails, primarily due to limited access to comprehensive clinical tools, particularly for syndro...
Main Authors: | Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hager Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, Crystel Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2024-04-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2024.1384094/full |
Similar Items
-
Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing
by: Ismail Gouiza, et al.
Published: (2024-01-01) -
Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy
by: Stéphane Zaffran, et al.
Published: (2023-02-01) -
Editorial: Advances in social cognition assessment and intervention in autism spectrum disorder
by: Soumeyya Halayem, et al.
Published: (2022-08-01) -
Toward an integrative socio-cognitive approach in autism spectrum disorder: NEAR method adaptation—study protocol
by: Jihene Bahri, et al.
Published: (2023-05-01) -
Immunity in the Progeroid Model of Cockayne Syndrome: Biomarkers of Pathological Aging
by: Khouloud Zayoud, et al.
Published: (2024-02-01)