Genetic diseases in otolaryngology

Molecular genetics is a rapidly expanding field with possibilities for novel diagnostic and treatment strategies for otorhinolaryngological diseases. Congenital hearing loss is the most common abnormality in the new born. Genetic factors contribute to about 50–60% of otorhinolaryngological disorders.  Allelic mutations in some genes can cause recessive and dominant mutations in the same gene or may cause syndromic or non- syndromic hearing loss and allergic reactions.
 
  • Cystic Fibrosis
  • Cleft Lip and Palate
  • Human Papilloma Virus
  • Thyroid Carcinoma
  • Salivary Gland Neoplasms
  • Acoustic Neuroma
  • Congenital Hearing Loss
  • Waardenberg’s Syndrome
  • Usher’s Syndrome
  • Pendred’s Syndrome
  • Alport’s Syndrome

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