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 language | English (US) |
|---|---|
| Pages (from-to) | 193-199 |
| Number of pages | 7 |
| Journal | Annals of Otology, Rhinology and Laryngology |
| Volume | 91 |
| Issue number | 2 I |
| State | Published - 1982 |
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ASJC Scopus subject areas
- Otorhinolaryngology
Cite this
Vaterite otoconia in two cases of otoconial membrane dysplasia. / Wright, C. G.; Rouse, R. C.; Johnsson, L. G.; Weinberg, A. G.; Hubbard, D. G.
In: Annals of Otology, Rhinology and Laryngology, Vol. 91, No. 2 I, 1982, p. 193-199.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Vaterite otoconia in two cases of otoconial membrane dysplasia
AU - Wright, C. G.
AU - Rouse, R. C.
AU - Johnsson, L. G.
AU - Weinberg, A. G.
AU - Hubbard, D. G.
PY - 1982
Y1 - 1982
N2 - 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.
AB - 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.
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UR - http://www.scopus.com/inward/citedby.url?scp=0020044966&partnerID=8YFLogxK
M3 - Article
C2 - 6123288
AN - SCOPUS:0020044966
VL - 91
SP - 193
EP - 199
JO - Annals of Otology, Rhinology and Laryngology
JF - Annals of Otology, Rhinology and Laryngology
SN - 0003-4894
IS - 2 I
ER -