Recessive Microtia, Meatal Atresia, and Hearing Loss

Report of a Sibship

Bruce W. Konigsmark, George T. Nager, Harriet L. Haskins

Research output: Contribution to journalArticle

Abstract

One of two brothers had bilateral and the other had unilateral microtia, meatal atresia, and significant hearing impairment. Reconstruction of the auricles was moderately successful. Temporal bone tomograms on one boy showed absent external canals, abnormal ossicles, and small middle ears. The inner ears were normal. These sibs probably have a recessively inherited syndrome described by Ellwood et al in two siblings and characterized by microtia, meatal atresia, and hearing loss.

Original languageEnglish (US)
Pages (from-to)105-109
Number of pages5
JournalArchives of Otolaryngology
Volume96
Issue number2
DOIs
StatePublished - 1972

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Hearing Loss
Siblings
Temporal Bone
Middle Ear
Inner Ear
Congenital Microtia

ASJC Scopus subject areas

  • Otorhinolaryngology

Cite this

Recessive Microtia, Meatal Atresia, and Hearing Loss : Report of a Sibship. / Konigsmark, Bruce W.; Nager, George T.; Haskins, Harriet L.

In: Archives of Otolaryngology, Vol. 96, No. 2, 1972, p. 105-109.

Research output: Contribution to journalArticle

Konigsmark, Bruce W. ; Nager, George T. ; Haskins, Harriet L. / Recessive Microtia, Meatal Atresia, and Hearing Loss : Report of a Sibship. In: Archives of Otolaryngology. 1972 ; Vol. 96, No. 2. pp. 105-109.
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