Hearing Loss and M.1555a>G Mitochondrial Mutation

Guilherme Machado de Carvalho
Guilherme Machado de Carvalho
Universidade Estadual de Campinas (UNICAMP) Universidade Estadual de Campinas (UNICAMP)

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Hearing Loss and M.1555a>G Mitochondrial Mutation

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References

22 Cites in Article
  1. Amiel Dror,Karen Avraham (2009). Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology.
  2. Nele Hilgert,Richard Smith,Guy Van Camp (2009). Forty-six genes causing nonsyndromic hearing impairment: Which ones should be analyzed in DNA diagnostics?.
  3. Haris Kokotas,Maria Grigoriadou,George Korres,Elisabeth Ferekidou,Eleftheria Papadopoulou,Polyxene Neou,Aglaia Giannoulia-Karantana,Dimitrios Kandiloros,Stavros Korres,Michael Petersen (2009). The A1555G mitochondrial DNA mutation in Greek patients with non-syndromic, sensorineural hearing loss.
  4. Toni Prezant,John Agapian,M Bohlman,Xiangdong Bu,Sitki Öztas,Wei-Qin Qiu,Kathleen Arnos,Gino Cortopassi,Lutfi Jaber,Jerome Rotter,Mordechai Shohat,Nathan Fischel-Ghodsian (1993). Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness.
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  9. Del Castillo,F Rodríguez-Ballesteros,M Alvarez,A Hutchin,T Leonardi,E De Oliveira,C (2005). A novel deletion involving the connexin-30 gene, del(GJB6-D13S1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.
  10. R Mingroni-Netto,R Abreu-Silva,Mcc Braga,K Lezirovitz,Della-Rosa Va (2001). Mitochondrial mutation A1555G (12S rRNA) and connexin 26 35delG mutation are frequent causes of deafness in Brazil.
  11. Altair Pupo,Sulene Pirana,Mauro Spinelli,Karina Lezirovitz,Regina Netto,Lisandra Macedo (2008). Study of a Brazilian Family Presenting Non-syndromic hearing loss with mitochondrial inheritance.
  12. Peter King,Xiaomei Ouyang,Lilin Du,Denise Yan,Simon Angeli,Xue Liu (2012). Etiologic Diagnosis of Nonsyndromic Genetic Hearing Loss in Adult vs Pediatric Populations.
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  15. C Wu,Y Chiu,P Chen,C Hsu (2007). Prevalence and Clinical Features of the Mitochondrial m.1555AA>G Mutation in Taiwanese Patients with Idiopatic Sensorineural Hearing Loss and Association of Haplogroup F with Low Penetrance in Three Families.
  16. Tianbin Chen,Qicai Liu,Ling Jiang,Can Liu,Qishui Ou (2013). Mitochondrial COX2 G7598A Mutation May Have a Modifying Role in the Phenotypic Manifestation of Aminoglycoside Antibiotic-Induced Deafness Associated with 12S rRNA A1555G Mutation in a Han Chinese Pedigree.
  17. C Angulo,J Gallo-Teran,B Senaris,A Fontalva,R Gonzalez-Aguado,J Fernandez-Luna (2011). Prevalence of the A1555G MTDNA mutation in sporadic hearing-impaired patients without known history of aminoglycosides treatment.
  18. G Paludetti,G Conti,Di Nardo,W,De Corso,E Rolesi,R Picciotti,P (2012). Infant hearing loss: from diagnosis to therapy.
  19. Pasquale Marsella,Alessandro Scorpecci,Concettina Pacifico,Fabio Presuttari,Sergio Bottero (2012). Pediatric BAHA in Italy: the “Bambino Gesù” Children’s Hospital’s experience.
  20. Maurizio Barbara,Vito Manni,Simonetta Monini (2009). Totally implantable middle ear device for rehabilitation of sensorineural hearing loss: preliminary experience with the Esteem®, Envoy.
  21. Mario Svirsky,Su-Wooi Teoh,Heidi Neuburger (2004). Development of Language and Speech Perception in Congenitally, Profoundly Deaf Children as a Function of Age at Cochlear Implantation.
  22. Mark Parker (2011). Biotechnology in the Treatment of Sensorineural Hearing Loss: Foundations and Future of Hair Cell Regeneration.

Funding

No external funding was declared for this work.

Conflict of Interest

The authors declare no conflict of interest.

Ethical Approval

No ethics committee approval was required for this article type.

Data Availability

Not applicable for this article.

How to Cite This Article

Guilherme Machado de Carvalho. 1970. \u201cHearing Loss and M.1555a>G Mitochondrial Mutation\u201d. Global Journal of Medical Research - J: Dentistry & Otolaryngology GJMR-J Volume 15 (GJMR Volume 15 Issue J1).

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Journal Specifications

Crossref Journal DOI 10.17406/gjmra

Print ISSN 0975-5888

e-ISSN 2249-4618

Keywords
Classification
GJMR-J Classification NLMC Code: WV 270
Version of record

v1.2

Issue date
May 23, 2015

Language
en
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Hearing Loss and M.1555a>G Mitochondrial Mutation

Guilherme Machado de Carvalho
Guilherme Machado de Carvalho <p>Universidade Estadual de Campinas (UNICAMP)</p>

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