Hostname: page-component-8448b6f56d-jr42d Total loading time: 0 Render date: 2024-04-25T03:35:36.842Z Has data issue: false hasContentIssue false

A dominant hereditary ossicular anomaly: bilateral incus anomaly and stapes fixation

Published online by Cambridge University Press:  28 January 2009

J H Lee*
Affiliation:
Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Hallym University, Chuncheon, South Korea
S H Jung
Affiliation:
Department of Otorhinolaryngology-Head and Neck Surgery, Wonju College of Medicine, Yonsei University, Wonju, South Korea
H C Kim
Affiliation:
Department of Radiology, School of Medicine, Hallym University, Chuncheon, South Korea
C H Park
Affiliation:
Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Hallym University, Chuncheon, South Korea
S M Hong
Affiliation:
Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, Hallym University, Chuncheon, South Korea
*
Address for correspondence: Dr J H Lee, Department of Otorhinolaryngology-Head and Neck Surgery, Chuncheon Sacred Heart Hospital, School of Medicine, Hallym University, 153 Kyo-Dong, Chuncheon, Kangwon, South Korea. Fax: 82 33 241 2909 E-mail: zoonox@nate.com

Abstract

Objective:

We report three generations of one family suffering from bilateral conductive hearing loss due to a congenital anomaly of the incus and stapes fixation.

Case report:

All three female patients presented with similar symptoms and findings of hearing impairment since birth. Their computed tomography findings were the same. An abnormally shaped incus, fixed stapes and hanging tympanic portion of the facial nerve were seen at surgery. Stapedotomy could not be performed because the hanging facial nerve blocked the operating field.

Conclusion:

Although several cases of familial ossicular anomaly have been reported, this is the first report of an incus anomaly and stapes fixation combined with a facial nerve anomaly.

Type
Clinical Records
Copyright
Copyright © JLO (1984) Limited 2009

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1Wehrs, RE. Congenital absence of the long process of the incus. Laryngoscope 1999;109:192–7CrossRefGoogle ScholarPubMed
2Higashi, K, Yamakawa, K, Itani, O, Togawa, K. Familial ossicular malformations: case report and review of literature. Am J Med Genet 1987;28:655–9CrossRefGoogle ScholarPubMed
3Kinsella, JB, Kerr, AG. Familial stapes superstructure fixation. J Laryngol Otol 1993;107:36–8CrossRefGoogle ScholarPubMed
4Thies, C, Handrock, M, Sperling, K, Rcis, A. Possible autosomal recessive inheritance of progressive hearing loss with stapes fixation. J Med Genet 1996;33:597–9CrossRefGoogle ScholarPubMed
5Hara, A, Ase, Y, Kusakari, J, Kurosaki, Y. Dominant hereditary conductive hearing loss due to an ossified stapedius tendon. Arch Otolaryngol Head Neck Surg 1997;123:1133–5CrossRefGoogle Scholar
6Doi, T, Nakazawa, H, Adachi, M, Kaneko, T, Munemoto, Y, Komeda, M et al. Familial isolated stapes-pyramidal fixation by a bony bar with normal stapedius tendon. Arch Otolaryngol Head Neck Surg 2005;131:349–52CrossRefGoogle ScholarPubMed
7Carlson, DL, Reeh, HL. X-linked mixed hearing loss with stapes fixation: case reports. J Am Acad Audiol 1993;4:420–5Google ScholarPubMed
8Snik, AF, Hombergen, GC, Mylanus, EA, Cremers, CW. Air-bone gap in patients with X-linked stapes gusher syndrome. Am J Otol 1995;16:241–6Google ScholarPubMed
9Cremers, CW, Snik, AF, Huygen, PL, Joosten, FB, Cremers, FP. X-linked mixed deafness syndromes with congenital fixation of the stapedial footplate and perilymphatic gusher (DFN3). Adv Otorhinolaryngol 2002;61:161–7Google ScholarPubMed