Articles

Genetics of Mondini Malformation

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Zheng Y, Schachern PA, Cureoglu S, Mutlu C, Dijalilian bH, Paparella MM. The shortened cochlea: its classification and histopathologic features. Int J Pediatr Otorhinolaryngol 2002;63:29e39.

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.

Gharib B, Esmaeili S, Shariati G, Mazloomi Nobandegani N, Mehdizadeh M. Recurrent bacterial meningitis in a child with hearing impairment, Mondini dysplasia: a case report. Acta Med Iran 2012;50(12):843-5.

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.

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