A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

被引:24
|
作者
Imtiaz, Faiqa [1 ]
Taibah, Khalid [2 ]
Ramzan, Khushnooda [1 ]
Bin-Khamis, Ghada [3 ]
Kennedy, Shelley [4 ]
Al-Mubarak, Bashayer [1 ]
Trabzuni, Daniah [1 ]
Allam, Rabab [1 ]
Al-Mostafa, Abeer [1 ]
Sogaty, Sameera [5 ]
Al-Shaikh, Abdulmoneem H. [6 ]
Bamukhayyar, Saeed S. [7 ]
Meyer, Brian F. [1 ]
Al-Owain, Mohammed [8 ,9 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Genet, Riyadh 11211, Saudi Arabia
[2] ENT Med Ctr, Riyadh 11333, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Dept Otolaryngol, Riyadh 11211, Saudi Arabia
[4] Childrens Hosp Eastern Ontario, Ontario Newborn Screening Program, Ottawa, ON K1H 8L1, Canada
[5] King Fahad Hosp, Med Genet Unit, Jeddah 21196, Saudi Arabia
[6] King Fahad Hosp, ENT Dept, Jeddah 21196, Saudi Arabia
[7] King Fahad Cent Hosp, Audiovestibular Med Unit, Jeddah 21196, Saudi Arabia
[8] King Faisal Specialist Hosp & Res Ctr, Dept Med Genet, Riyadh 11211, Saudi Arabia
[9] Al Faisal Univ, Coll Med, Riyadh 11533, Saudi Arabia
关键词
RECESSIVE DEAFNESS; MUTATIONS;
D O I
10.1186/1471-2350-12-91
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Hearing loss is a clinically and genetically heterogeneous disorder. Mutations in the DFNB1 locus have been reported to be the most common cause of autosomal recessive non-syndromic hearing loss worldwide. Apart from DFNB1, many other loci and their underlying genes have also been identified and the basis of our study was to provide a comprehensive introduction to the delineation of the molecular basis of non-syndromic hearing loss in the Saudi Arabian population. This was performed by screening DFNB1 and to initiate prioritized linkage analysis or homozygosity mapping for a pilot number of families in which DFNB1 has been excluded. Methods: Individuals from 130 families of Saudi Arabian tribal origin diagnosed with an autosomal recessive non-syndromic sensorineural hearing loss were screened for mutations at the DFNB1 locus by direct sequencing. If negative, genome wide linkage analysis or homozygosity mapping were performed using Affymetrix GeneChip (R) Human Mapping 250K/6.0 Arrays to identify regions containing any known-deafness causing genes that were subsequently sequenced. Results: Our results strongly indicate that DFNB1 only accounts for 3% of non-syndromic hearing loss in the Saudi Arabian population of ethnic ancestry. Prioritized linkage analysis or homozygosity mapping in five separate families established that their hearing loss was caused by five different known-deafness causing genes thus confirming the genetic heterogeneity of this disorder in the kingdom. Conclusion: The overall results of this study are highly suggestive that underlying molecular basis of autosomal recessive non-syndromic deafness in Saudi Arabia is very genetically heterogeneous. In addition, we report that the preliminary results indicate that there does not seem to be any common or more prevalent loci, genes or mutations in patients with autosomal recessive non-syndromic hearing loss in patients of Saudi Arabian tribal origin.
引用
收藏
页数:6
相关论文
共 50 条
  • [11] Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population
    Morgan, Anna
    Lenarduzzi, Stefania
    Spedicati, Beatrice
    Cattaruzzi, Elisabetta
    Murru, Flora Maria
    Pelliccione, Giulia
    Mazza, Daniela
    Zollino, Marcella
    Graziano, Claudio
    Ambrosetti, Umberto
    Seri, Marco
    Faletra, Flavio
    Girotto, Giorgia
    GENES, 2020, 11 (11) : 1 - 16
  • [12] The genetic bases for non-syndromic hearing loss among Chinese
    Xiao Mei Ouyang
    Denise Yan
    Hui Jun Yuan
    Dai Pu
    Li Lin Du
    Don Yi Han
    Xue Zhong Liu
    Journal of Human Genetics, 2009, 54 : 131 - 140
  • [13] The genetic bases for non-syndromic hearing loss among Chinese
    Ouyang, Xiao Mei
    Yan, Denise
    Yuan, Hui Jun
    Pu, Dai
    Du, Li Lin
    Han, Don Yi
    Liu, Xue Zhong
    JOURNAL OF HUMAN GENETICS, 2009, 54 (03) : 131 - 140
  • [14] Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
    Cabanillas, Ruben
    Dineiro, Marta
    Cifuentes, Guadalupe A.
    Castillo, David
    Pruneda, Patricia C.
    Alvarez, Rebeca
    Sanchez-Duran, Noelia
    Capin, Raquel
    Plasencia, Ana
    Viejo-Diaz, Monica
    Garcia-Gonzalez, Noelia
    Hernando, Ines
    Llorente, Jose L.
    Reparaz-Andrade, Alfredo
    Torreira-Banzas, Cristina
    Rosell, Jordi
    Govea, Nancy
    Ramon Gomez-Martinez, Justo
    Nunez-Batalla, Faustino
    Garrote, Jose A.
    Mazon-Gutierrez, Angel
    Costales, Maria
    Isidoro-Garcia, Maria
    Garcia-Berrocal, Belen
    Ordonez, Gonzalo R.
    Cadinanos, Juan
    BMC MEDICAL GENOMICS, 2018, 11
  • [15] Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
    Rubén Cabanillas
    Marta Diñeiro
    Guadalupe A. Cifuentes
    David Castillo
    Patricia C. Pruneda
    Rebeca Álvarez
    Noelia Sánchez-Durán
    Raquel Capín
    Ana Plasencia
    Mónica Viejo-Díaz
    Noelia García-González
    Inés Hernando
    José L. Llorente
    Alfredo Repáraz-Andrade
    Cristina Torreira-Banzas
    Jordi Rosell
    Nancy Govea
    Justo Ramón Gómez-Martínez
    Faustino Núñez-Batalla
    José A. Garrote
    Ángel Mazón-Gutiérrez
    María Costales
    María Isidoro-García
    Belén García-Berrocal
    Gonzalo R. Ordóñez
    Juan Cadiñanos
    BMC Medical Genomics, 11
  • [16] Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss
    Lu, Yajie
    Yao, Jun
    Wei, Qinjun
    Xu, Jin
    Xing, Guangqian
    Cao, Xin
    INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2018, 105 : 6 - 11
  • [17] non-syndromic hearing loss causative genesManisha
    Ray, Manisha
    Sarkar, Saurav
    Sable, Mukund Namdev
    BIOSCIENCE REPORTS, 2021, 41 (10)
  • [18] Non-Syndromic Sensorineural Hearing Loss in Children
    Robson, Caroline D.
    Lewis, Martin
    D'Arco, Felice
    NEUROIMAGING CLINICS OF NORTH AMERICA, 2023, 33 (04) : 531 - 542
  • [19] Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review
    Alde, Mirko
    Cantarella, Giovanna
    Zanetti, Diego
    Pignataro, Lorenzo
    La Mantia, Ignazio
    Maiolino, Luigi
    Ferlito, Salvatore
    Di Mauro, Paola
    Cocuzza, Salvatore
    Lechien, Jerome Rene
    Iannella, Giannicola
    Simon, Francois
    Maniaci, Antonino
    BIOMEDICINES, 2023, 11 (06)
  • [20] Peripheral Vestibular Dysfunction Is a Common Occurrence in Children With Non-syndromic and Syndromic Genetic Hearing Loss
    Wang, Alicia
    Shearer, A. Eliot
    Zhou, Guang Wei
    Kenna, Margaret
    Poe, Dennis
    Licameli, Greg R.
    Brodsky, Jacob R.
    FRONTIERS IN NEUROLOGY, 2021, 12