Vaterite Otoconia in Two Cases of Otoconial Membrane Dysplasia

C. G. Wright, R. C. Rouse, L. G. Johnsson, A. G. Weinberg, D. G. Hubbard

Research output: Contribution to journalArticle

14 Scopus citations

Abstract

Scanning electron microscopy, electron microprobe analysis, and x-ray powder diffraction were used to study temporal bone specimens obtained at autopsy from an infant with Potter syndrome and from a second trimester fetus, which was the product of an elective abortion. The mothers of both the infant and fetus were juvenile-onset rheumatoid arthritis patients who took prostaglandin inhibitors during pregnancy. The infant's external ears were low set and the left ear canal was stenotic. The vestibular maculae on the left were covered by aberrant otoconia composed of vaterite. In the right inner ear, otoconia were entirely absent, although the gelatinous otoconial membranes were intact. Only the left saccule and right utricle from the fetus were studied; both contained vaterite crystals similar to those in the infant. In addition, apatite was present in the fetal utricle, apparently lying on the macula beneath the vaterite otoconia.

Original languageEnglish (US)
Pages (from-to)193-199
Number of pages7
JournalAnnals of Otology, Rhinology & Laryngology
Volume91
Issue number2
DOIs
StatePublished - Mar 1982

ASJC Scopus subject areas

  • Otorhinolaryngology

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    Wright, C. G., Rouse, R. C., Johnsson, L. G., Weinberg, A. G., & Hubbard, D. G. (1982). Vaterite Otoconia in Two Cases of Otoconial Membrane Dysplasia. Annals of Otology, Rhinology & Laryngology, 91(2), 193-199. https://doi.org/10.1177/000348948209100215