D0004
DEAF (Maternally Inherited Deafness or Aminoglycoside-induced Deafness) Mitochondrial disease
Test Details: Aminoglycoside are a group of pharmacologic agents that have been shown to have toxic effects to the cochleovestibular system. Predisposition to aminoglycoside induced deafness, caused by aminoglycoside exposure is known to be associated with pathogenic variants in the MT-RNR1 gene. Non-syndromic mitochondrial hearing loss and deafness is transmitted by maternal inheritance.
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Category
Molecular Genetics
Pre-test Information
Clinical and family history is required.
Report Delivery
4 working days
Gender
All
Organ
Ear
DEAF (Maternally Inherited Deafness or Aminoglycoside-induced Deafness) Mitochondrial disease
4400
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