Biomedical subjects
S Pruzansky
Publications and source records attributed to S Pruzansky.
Prevalence of arch collapse and malocclusion in complete unilateral cleft lip and palate.
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Oral-facial-digital syndrome in a negro female.
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Effects of stimulus content and duration on talker identification.
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Is roentgencephalometry being fully exploited as an instrument for clinical investigation?
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Intellectual development and the OFD syndrome: a review.
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Roentgencephalometric studies of tonsils and adenoids in normal and pathologic states.
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Dental abnormalities in the deciduous and permanent dentitions of individuals with cleft lip and palate.
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Bilateral asymmetry in mandibular tooth development.
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Validity of the birth certificate in the epidemiologic assessment of facial clefts.
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Postnatal development of craniofacial malformations.
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The "Stretch Factor" in soft palate function.
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Disseminate pigmented nevi and short stature.
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CT in the evaluation of the orbit and the bony interorbital distance.
The distance between the orbits and their individual dimensions are important in the diagnosis of craniofacial anomalies. Most observers rely on standard radiographs for measuring the bony interorbital distance. Tomography of the skull base and orbital computed tomography (CT) can also be used. This article describes the normal range of the bony interorbital distance and other useful orbital linear and angular measurements as determined from a series of CT scans of the orbits in 400 adults who had CT for other purposes. The normal interorbital distance measured at the posterior border of the frontal processes of the maxilla on nonrotated scans, in the plane of the optic nerve, ranges from 2.29 to 3.21 cm (average, 2.67 cm) in men and 2.29 to 3.20 cm (average, 2.56 cm) in women. The widest interorbital distance lies behind the posterior poles of the globes. This ranges from 3.16 to 4.10 cm (average, 3.37 cm) in men and 2.93 to 3.67 cm (average, 3.20 cm) in women.
The otologic manifestations of mandibulofacial dysostosis.
Sixteen patients (32 ears) with diagnoses of mandibulofacial dysostosis were reviewed. The characteristic otologic manifestations of the syndrome were delineated, found to be bilateral, and consist of the following: 1. Mild symmetric deformity of the auricle (grade 1 microtia). 2. Agenesis or hypoplastic development of the mastoid and mastoid antrum. 3. Absence of the external auditory canal. 4. Marked narrowing or agenesis of the middle ear cleft. 5. Agenesis or severe malformation of the malleus and incus. When present, the malleus and incus are most often rudimentary, fused to form a conglomerate mass, and ankylosed to either the atretic plate, epitympanum, or both. 6. Stapedial malformations which usually consist of a deformed suprastructure. 7. Frequently the tegmen assumes a more inferior (low lying) position than normal. 8. Occasionally, the facial nerve pursues an abnormal course and is located more anteriorly than would be expected. 9. A normal inner ear. 10. Normal bone conduction with a marked (greater than 50 dB) conductive hearing loss. 11. Marked disparity between the degree of auricular deformity (mild; grade 1 microtia) and the degree of deformity of the remaining first and second branchial arch derivatives that constitute the external and middle ears (severe).