Ear, Nose & Throat
Addresses genetic factors related to hearing loss, including both syndromic and non-syndromic cases, with a focus on genes associated with autosomal recessive and dominant forms. It also includes genes linked to various syndromes like Alport, Pendred, Waardenburg, Usher, and branchio-oto-renal.
- TAT : 28 working days
- Sample : EDTA blood
Included Syndromes & Disorders
- Alport syndrome
- Coffin-Lowry snydrome
- Deafness autosomal recessive and dominant
- Non-syndromic hearing loss
- Pendred syndrome
- Perrault syndrome
- Pfeiffer syndrome
- Sensorineural hearing loss
- Stickler syndrome
- Syndromic hearing loss
- Usher syndrome
- Waardenburg syndrome
- Wolfram syndrome
