Abstract
Achondroplasia is an autosomal dominant dysplasia of the skeleton; the main features are shortness of the limbs, cranio-facial and odonto-maxillary anomalies and prominent forehead.
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References
G. Cianfrone, M. A. Nistico, R. Turchetta, Acondroplasia e sordità infantile: tre casi. La Nuova Clin. ORL XXXIV 193:195 (1982).
L. Glass, I. Shapiro, S. E. Hodge, L. Bergstrom and D. L. Rimoin, Audiological findings of patients with achondroplasia. Int. J. Fed. Otorhinolaryng. 3, 129:135 (1981).
J. Hall, Unpublished survey of 150 patients with achondroplasia, ref. L. Glass et al. (1974).
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© 1988 Plenum Press, New York
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Pinelli, V., Masi, R., Partipilo, P., Pierro, V., Tieri, L. (1988). Otologic Impairments in Achondroplasia: A Nosologic Assessment. In: Nicoletti, B., Kopits, S.E., Ascani, E., McKusick, V.A., Dryburgh, S.C. (eds) Human Achondroplasia. Basic Life Sciences, vol 48. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-8712-1_20
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DOI: https://doi.org/10.1007/978-1-4684-8712-1_20
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4684-8714-5
Online ISBN: 978-1-4684-8712-1
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