Genetics of Mondini Malformation

  • Rozita Jalilian Research Center for Immunodeficiencies, Children’s Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran.
  • Nima Rezaei Research Center for Immunodeficiencies, Children’s Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, Iran. AND Molecular Immunology Research Center; and Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
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Abstract

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References

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Çiftdoğan DY, Bayram N, Özdemir Y, Bayraktaroğlu S, Vardar F. A case of Mondini dysplasia with recurrent Streptococcus pneumoniae meningitis. Eur J Pediatr 2009;168:1533-5.

Lin CY, Lin HC, Peng CC, Lee KS, Chiu NC. Mondini dysplasia presenting as otorrhea without meningitis. Pediatr Neonat 2012;53:371e373.

Aghamohammadi A, Abolhassani H, Mohammadinejad P, Rezaei N. The approach to children with recurrent infections. Iran J Allergy Asthma Immunol 2012;11(2):89-109.

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Wu CC, Yeh TH, Chen PJ, Hsu CJ. Prevalent SLC26A4 mutations in patients with enlarged vestibular aqueduct and/or Mondini dysplasia: a unique spectrum of mutations in Taiwan, including a frequent founder mutation. Laryngoscope 2005;115(6):1060-4.

Fitoz S, Sennaroglu L, Incesulu A, Cengiz FB, Koc¸ Y, Tekin M. SLC26A4 mutations are associated with a specific inner ear malformation. Int J Pediatr Otorhinolaryngol 2007;71:479e86.

How to Cite
1.
Jalilian R, Rezaei N. Genetics of Mondini Malformation. Acta Med Iran. 51(5):345-346.
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