Usher syndrome is a heterogeneous autosomal recessive trait and the most common cause of hereditary deaf-blindness. Usher syndrome type I (USH1) is characterised by profound congenital sensorineural hearing loss, vestibular dysfunction, and prepubertal onset of retinitis pigmentosa. Of the at least
Clinical findings in obligate carriers of type I Usher syndrome
✍ Scribed by Wagenaar, M. ;ter Rahe, B. ;van Aarem, A. ;Huygen, P. ;Admiraal, R. ;Bleeker-Wagemakers, E. ;Pinckers, A. ;Kimberling, W. ;Cremers, C.
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 487 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0148-7299
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