Microtia in a Large White Yorkshire Piglet - A Case Report
DOI:
https://doi.org/10.5455/ijlr.20200924110314%20%20%20%20%20Keywords:
Aural atresia, Congenital anomaly, Large White Yorkshire, Microtia, PigletAbstract
Microtia condition was observed in a Large White Yorkshire (LWY) piglet in an organized piggery farm at Kattupakkam, Chengalpattu district of Tamil Nadu, India. Although this condition is well documented in human beings. To the best of our knowledge, this is a unique case report on the incidence of congenital microtia with aural atresia in a LWY piglet.
References
Alasti, F. and. Van Camp, G. (2009). Genetics of microtia and associated syndromes. Journal of Medical Genetics, 46(6): 361-369.
Gendron, C., Schwentker, A. and van Aalst, J.A. (2016). Genetic Advances in Craniofacial Malformations: Genetic Advances in the Understanding of Microtia. Journal of Pediatric Genetics, 5(4): 189-97.
Luquetti, D.V., Heike, C.L., Hing, A.V., Cunningham, M. L. and Cox, T. C. (2012). Microtia: epidemiology and genetics. American Journal of Medical Genetics Part A, 158(1): 124-139.
Kalam, M.A. and Ahmed, T. (2013). A short review on microtia and Bangladesh perspective. Bangladesh Journal of Plastic Surgery, 4(1): 1-3.
Marchegiani, S., Davis, T., Tessadori, F., Van Haaften, G., Brancati, F., Hoischen, A., Huang, H., Valkanas, E., Pusey, B., Schanze, D. and Venselaar, H. (2015). Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and Barber-Say syndromes. The American Journal of Human Genetics, 97(1): 99-110.
Marx, H. (1926). Die Missbildungen des ohres. In Die Krankheiten des Gehörorgans (pp. 131-169). Springer, Berlin, Heidelberg.
Qiao, R., He, Y., Pan, B., Xiao, S., Zhang, X., Li, J., Zhang, Z., Hong, Y., Xing, Y. and Ren, J. (2015). Understanding the molecular mechanisms of human microtia via a pig model of HOXA1 syndrome. Disease Models & Mechanisms, 8(6): 611-622.
Rezaei, M., Mahmoudi, T., Ebrahimi, M., & Vosugh, D. (2015). First report of microtia in dog. Comparative Clinical Pathology, 24(3): 699-702.
Sanchez, O., Méndez, J.R., Gomez, E. and Guerra, D. (1997). Clinico-epidemiologic study of microtia. Investigacion clinica, 38(4): 203-217.
Suutarla, S., Rautio, J., Ritvanen, A., Ala-Mello, S., Jero, J. and Klockars, T. (2007). Microtia in Finland: comparison of characteristics in different populations. International Journal of Pediatric Otorhinolaryngology, 71(8): 1211-1217.
Tekes, A., Ishman, S.L., Baugher, K.M., Brown, D.J., Lin, S.Y., Tunkel, D.E., Unalp-Arida, A. and Huisman, T.A. (2013). Does microtia predict severity of temporal bone CT abnormalities in children with persistent conductive hearing loss? Journal of Neuroradiology, 40(3): 192-197.
Wang, R.Y., Earl, D.L., Ruder, R.O. and Graham, J.M. (2001). Syndromic ear anomalies and renal ultrasounds. Pediatrics, 108(2): e32-e32.
Wang, P., Wang, Y., Fan, X., Liu, Y., Fan, Y., Liu, T., Chen, C., Zhang, S. and Chen, X., (2019). Identification of sequence variants associated with severe microtia-astresia by targeted sequencing. BMC Medical Genomics, 12(1): 28.
Downloads
Published
How to Cite
Issue
Section
License

This work is licensed under a Creative Commons Attribution 4.0 International License.
