Molecular genetic advances in semicircular canal abnormalities and sensorineural hearing loss: A report of 16 cases

Otolaryngology - Head and Neck Surgery

Volumn 129, Issue 6, 2003, Pages 637-646

  Yu, Kathy K ^a   Mukherji, Suresh ^b,c   Carrasco, Vincent ^a   Pillsbury, Harold C ^a   Shores, Carol G ^a  

^a UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF NORTH CAROLINA   (United States)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; APLASIA; AUDIOGRAPHY; AUDIOMETRY; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COCHLEA; COCHLEA MALFORMATION; COMPUTER ASSISTED TOMOGRAPHY; DISEASE SEVERITY; DYSPLASIA; EMBRYOLOGY; GENE MUTATION; HUMAN; INNER EAR MALFORMATION; MIDDLE EAR MALFORMATION; MOLECULAR GENETICS; PATHOLOGICAL ANATOMY; PERCEPTION DEAFNESS; PURE TONE AUDIOMETRY; REVIEW; SEMICIRCULAR CANAL; SEMICIRCULAR CANAL APLASIA; SEMICIRCULAR CANAL DYSPLASIA; SEMICIRCULAR CANAL MALFORMATION; SPEECH; SYNDROME DELINEATION; TERATOLOGY;

EID: 0345529104     PISSN: 01945998     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0194-5998(03)01593-6     Document Type: Article

References (18)

1. Gulya AJ, Juhlin NR. Histopathology of deafness. ENT J 1992;71:494-502.
2. Jackler RK, Luxford WM, House WF. Congenital malformations of the inner ear: a classification based on embryogenesis. Laryngoscope 1987;97(suppl 40):2-14.
3. Parnes LS, Chernoff WG. Bilateral semicircular canal aplasia with near-normal cochlear development. Ann Otol Rhinol Laryngol 1990;99:957-9.
4. Antonelli PJ, Varela AE, Mancuso AA. Diagnostic yield of high-resolution computed tomography for pediatric sensorineural hearing loss. Laryngoscope 1999;109:1642-7.
5. Fekete DM. Development of the vertebrate ear: insights from knockouts and mutants. Trends Neurosci 1999;22:263-9.
6. Gavalas A, Studer M, Lumsden A, et al. Hoxa1 and Hoxb1 synergize in patterning the hindbrain, cranial nerves and second pharyngeal arch. Development 1998;125:1123-36.
7. McKay IJ, Lewis J, Lumsden A. The role of FGF-3 in early inner ear development: an analysis in normal and Kreisler mutant mice. Dev Biol 1996;174:370-8.
8. Hadrys T, Braun T, Rinkwitz-Brandt S, et al. Nkx5-1 controls semicircular canal formation in the mouse inner ear. Development 1998;125:33-9.
9. Torres M, Gomez-Pardo E, Gruss P. Pax2 contributes to inner ear patterning and optic nerve trajectory. Development 1996;122:3381-91.
10. Wang W, Van De Water T, Lufkin T. Inner ear and maternal reproductive effects in mice lacking the Hmx3 homeobox gene. Development 1998;125:621-34.
11. Salminen M, Meyer B, Bober E, et al. netrin1 is required for semicircular canal formation in the mouse inner ear. Development 2000;127:13-22.
12. Satar B, Mukherji SK, Telian SA, Congenital aplasia of the semicircular canals. Otol Neurotol 2003;24:437-46.
13. Moller CG, Kimberling WJ, Davenport SL, et al. Usher syndrome: an otoneurologic study. Laryngoscope 1989;99:73-9.
14. Smith RJ, Lee EC, Kimberling WJ, et al. Localization of 2 genes for Usher syndrome type 1 to chromosome 11. Genomics 1992;14:995-1002.
15. Morsli H, Tuorto F, Choo D, et al. Otx1 and Otx2 activities are required for the normal development of the mouse inner ear. Development 1999;126:2335-43.
16. tenBerge D, Brouwer A, Korving J, et al. Prx1 and Prx2 in skeletogenesis: roles in the craniofacial region, inner ear and limbs. Development 1998;125:3831-42.
17. Paparella MM. Mondini's deafness. A review of histopathology. Ann Otol Rhinol Laryngol 1980;89(suppl 67):1-10.
18. Ma Q, Chen Z, del Barco Barrantes I, et al. neurogenin I is essential for the determination of neuronal precursors for proximal cranial sensory ganglia. Neuron 1998;20:469-82.