Congenital absence of the long process of the incus

Laryngoscope

Volumn 109, Issue 2, 1999, Pages 192-197

  Wehrs, Roger E ^a  

^a UNIVERSITY OF OKLAHOMA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGENESIS; ARTICLE; AUDITORY OSSICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CHILD; CONDUCTION DEAFNESS; FEMALE; HUMAN; INCUS; MIDDLE EAR RECONSTRUCTION; PRIORITY JOURNAL; STAPES; X CHROMOSOME DOMINANT INHERITANCE;

ADULT; AUDIOMETRY, PURE-TONE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; HEARING LOSS, CONDUCTIVE; HUMANS; INCUS; OSSICULAR REPLACEMENT; OTOLOGIC SURGICAL PROCEDURES; PEDIGREE; POSTOPERATIVE CARE; SEVERITY OF ILLNESS INDEX; X CHROMOSOME;

EID: 0032976948     PISSN: 0023852X     EISSN: 15314995     Source Type: Journal    
DOI: 10.1097/00005537-199902000-00004     Document Type: Article

References (8)

1. Hough JVD. Malformations and anatomical variations seen in the middle ear during the operation for mobilization of the stapes. Laryngoscope 1958;68:1337-1379.
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3. Henner R, Buckingham R. The recognition and surgical treatment of congenital ossicular defects. Laryngoscope 1956;66:526-539.
4. Shea J, Daniel JO, John RE. Congenital absence of the incus: a novel method of reconstruction. Otolaryngol Head Neck Surg 1987;97:413-415.
5. Parsed U, Chin YH. Bilateral congenital absence of incus. J Laryngol Otol 1975;89:1265-1269.
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8. Wehrs RE. Surgical technique of homograft tympanoplasty. Otolaryngol Clin North Am 1977;10(3):517-527.