Hereditary congenital unilateral deafness: A new disorder?

Annals of Otology, Rhinology and Laryngology

Volumn 114, Issue 4, 2005, Pages 332-337

  Dikkers, Frederik G ^b   Verheij, Joke B G M ^b   Van Mechelen, Monique ^a,b  

^a University Medical Center Groningen ^*

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

Congenital deafness; Congenital hearing loss; Hereditary deafness; Hereditary hearing loss; Unilateral deafness; Unilateral hearing loss

Indexed keywords

ADULT; ARTICLE; BODY EQUILIBRIUM; CASE REPORT; CONGENITAL DEAFNESS; FAMILY; FEMALE; HEREDITARY CONGENITAL UNILATERAL DEAFNESS; HUMAN; MEDICAL LITERATURE; PRIORITY JOURNAL; VESTIBULAR DISORDER;

EID: 17244366907     PISSN: 00034894     EISSN: None     Source Type: Journal    
DOI: 10.1177/000348940511400414     Document Type: Article

References (14)

1. Niparko JK. The epidemiology of hearing loss - how prevalent is hearing loss? In: Niparko JK, Kirk KI, Mellon NK, Robbins AM, Tucci DL, Wilson BS, eds. Cochlear implants. Principles and practice. Philadelphia, Pa: Lippincott Williams & Wilkins, 2000:88-92.
2. Smith AB. Unilateral hereditary deafness. Lancet 1939; Dec 2:1172-3.
3. Everberg G. Hereditary unilateral deafness. Acta Otolaryngol (Stockh) 1957;47:303-11.
4. Everberg G. Further studies on hereditary unilateral deafness. Acta Otolaryngol (Stockh) 1960;51:615-35.
5. Brookhouser PE, Worthington DW, Kelly WJ. Unilateral hearing loss in children. Laryngoscope 1991;101:1264-72.
6. Graf K. Hereditary unilateral deaf-mutism as a variable manifestation of bilateral deaf-mutism or hearing loss [in German]. Laryngorhinootologie 1992;71:242-5.
7. Lina-Granade G, Collet L, Morgon A. Physiopathological investigations in a family with a history of unilateral hereditary deafness. Acta Otolaryngol (Stockh) 1995;115:196-201.
8. Grewel F, van den Horst A. Hereditary congenital deafness in uniovular twins. Acta Gerontol (Milano) 1959;8:99-116.
9. Jackler RK, Luxford WM, House WF. Congenital malformations of the inner ear: a classification based on embryogenesis. Laryngoscope 1987;97(suppl 40):2-14.
10. Popper AN, Hoxter B. Sensory and nonsensory ciliated cells in the ear of the sea lamprey, Petromyzon marinus. Brain Behav Evol 1987;30:43-61.
11. Parnes LS, Chernoff WG. Bilateral semicircular canal aplasia with near-normal cochlear development. Two case reports. Ann Otol Rhinol Laryngol 1990;99:957-9.
12. Yu KK, Mukherji S, Carrasco V, Pillsbury HC, Shores CG. Molecular genetic advances in semicircular canal abnormalities and sensorineural hearing loss: a report of 16 cases. Otolaryngol Head Neck Surg 2003;129:637-46.
13. Cargill EJ, Famula TR, Strain GM, Murphy KE. Genetic analyses of hereditary deafness: a canine model. In: Proceedings, Fourth Conference on the Molecular Biology of Hearing and Deafness. NIDCD/DRF, 2001:115.
14. Strain GM. Congenital deafness and its recognition. Vet Clin North Am Small Anim Pract 1999;29:895-907, vi.