Cochleosaccular dysplasia: A morphometric and histopathologic study in a series of temporal bones

Otology and Neurotology

Volumn 25, Issue 4, 2004, Pages 530-535

  Sampaio, Andre L L ^a,b   Cureoglu, Sebahattin ^c   Schachern, Patricia A ^b,c,e   Kusunoki, Takeshi ^b   Paparella, Michael M ^b,d   Oliveira, Carlos A C P ^a  

^a UNIVERSITY OF BRASILIA   (Brazil)

^b International Hearing Foundation   (United States)

^c UNIVERSITY OF MINNESOTA   (United States)

^d Paparella Ear Head and Neck Institute PA   (United States)

^e Lions Research Building ^*  (United States)

Author keywords

Cochleosaccular dysplasia; Histopathology; Scheibe's dysplasia

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CELL LOSS; CHILD; CLINICAL ARTICLE; COCHLEA DUCT; COCHLEOSACCULAR DYSPLASIA; CONTROLLED STUDY; CORTI ORGAN; FAMILY HISTORY; FEMALE; HAIR CELL; HEARING IMPAIRMENT; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; INNER EAR DISEASE; MALE; MORPHOMETRICS; MUTISM; NEWBORN; PRIORITY JOURNAL; SPIRAL GANGLION; STRIA VASCULARIS; TEMPORAL BONE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; ANALYSIS OF VARIANCE; BONE DISEASES, DEVELOPMENTAL; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; COCHLEA; DEAFNESS; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; LIGAMENTS; MALE; MIDDLE AGED; ORGAN OF CORTI; SACCULE AND UTRICLE; SPIRAL GANGLION; STRIA VASCULARIS; TEMPORAL BONE;

EID: 4043123473     PISSN: 15317129     EISSN: None     Source Type: Journal    
DOI: 10.1097/00129492-200407000-00021     Document Type: Article

References (22)

1. Paparella M, Schachern P. Sensorial neural hearing loss-nongenetic and genetic. In: Paparella M, Shumrick DA, Gluckman J, et al, eds. Otolaryngology. Philadelphia: WB Saunders Co, 1991:1561.
2. Scheibe A. A case of deaf-mutism, with auditory atrophy and anomalies of development in membranous labyrinth in both ears. Arch Otol 1892;21:12-22.
3. Scheibe A. Anomalies of development in the inner ear of a deaf-mute [in German]. Z Ohrenheil 1895;27:95-99.
4. Nomura Y, Kawabata I. Scheibe dysgenesis of the inner ear. J Laryngol Otol 1980;94:1345-1352.
5. Nadol JB, Burgess B. Cochleosaccular degeneration of the inner ear and progressive cataracts inherited as an autosomal dominant trait. Laryngoscope 1982;92:1028-1037.
6. Otte J, Schuknecht HF, Kerr GA. Ganglion cell population in normal and pathological human cochleas. Implication for cochlear implantation. Laryngoscope 1978;88:1231-1246.
7. Schuknecht HF. Techniques for study of cochlea function and pathology in experimental animals. Arch Otolaryngol 1953;58:377-397.
8. Hudson W, Ruben R. Hereditary deafness in the Dalmatian dog. Arch Otolaryngol 1962;75::213-219.
9. Hilding DA, Sugiura A, Nakai Y. Deaf white mink. Electron microscopic study of the inner ear. Ann Otol Rhinol Laryngol 1967;76:647-663.
10. Wilson T, Kane F. Congenital deafness in white cats. Acta Otolaryngol 1959;50:269-277.
11. Deol MS. The neural crest and the acoustic ganglion. J Embryol Exp Morphol 1967;17:533-541.
12. Anniko M. Specific pathology of the stria vascularis in postnatal progressive genetic inner ear disorder. Hear Res 1982;6:247-258.
13. Schuknecht HF. Pathology of the Ear. Cambridge, MA: Harvard University Press, 1974.
14. Walby PA, Schuknecht HF. Concomitant occurrence of cochleosaccular dysplasia and Down's syndrome. Arch Otolaryngol 1984;110:477-479.
15. Mills JH, Schmidt RA, Rulish LF. Age related changes in auditory potentials of mongolian gerbil. Hear Res 1990;46:201-210.
16. Schuknecht HF, Iagarashi M, Gacek RR. The pathological types of cochleosaccular degeneration. Acta Otolaryngol 1965;59:154-170.
17. Altamann F. Histologic picture of inherited nerve deafness in man and animals. Arch Otolaryngol 1950;51:852-890.
18. Hiraide F, Paparella M. Stria concretion in the inner ears of children. In: Nomura Y, ed. Hearing Loss and Dizziness. Tokyo, New York: Igaku-Shoin, 1985:100.
19. Lalwanil AK, Linthicum FH, Wilcox ER, et al. A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration. Audiol Neurotol 1997;2:139-154.
20. Igarashi M, MacRae D, O-Uchi T, et al. Cochleosaccular degeneration in one of three sisters with hereditary deafness, absent gastric motility, small bowel diverticulitis, and progressive sensory neuropathy. ORL J Otorhinolaryngol Relat Spec 1981;43:4-16.
21. Kikuchi K, Hilding DA. The defective organ of Corti in Shaker-I mice. Acta Otolaryngol 1965;60:287-303.
22. Lindsay JR, Caruthers DG, Harrison MS, et al. Inner ear pathology in children following maternal rubella. Ann Otol Rhinol Laryngol 1954;62:461-464.