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Yang, C. Auriculo-condylar Syndrome. Encyclopedia. Available online: https://encyclopedia.pub/entry/4861 (accessed on 22 September 2026).
Yang C. Auriculo-condylar Syndrome. Encyclopedia. Available at: https://encyclopedia.pub/entry/4861. Accessed September 22, 2026.
Yang, Catherine. "Auriculo-condylar Syndrome" Encyclopedia, https://encyclopedia.pub/entry/4861 (accessed September 22, 2026).
Yang, C. (2020, December 24). Auriculo-condylar Syndrome. In Encyclopedia. https://encyclopedia.pub/entry/4861
Yang, Catherine. "Auriculo-condylar Syndrome." Encyclopedia. Web. 24 December, 2020.
Auriculo-condylar Syndrome
Edit

Auriculo-condylar syndrome is a condition that affects facial development, particularly development of the ears and lower jaw (mandible).

genetic conditions

References

  1. Gordon CT, Vuillot A, Marlin S, Gerkes E, Henderson A, AlKindy A,Holder-Espinasse M, Park SS, Omarjee A, Sanchis-Borja M, Bdira EB, Oufadem M,Sikkema-Raddatz B, Stewart A, Palmer R, McGowan R, Petit F, Delobel B, SpeicherMR, Aurora P, Kilner D, Pellerin P, Simon M, Bonnefont JP, Tobias ES,García-Miñaúr S, Bitner-Glindzicz M, Lindholm P, Meijer BA, Abadie V, DenoyelleF, Vazquez MP, Rotky-Fast C, Couloigner V, Pierrot S, Manach Y, Breton S,Hendriks YM, Munnich A, Jakobsen L, Kroisel P, Lin A, Kaban LB, Basel-VanagaiteL, Wilson L, Cunningham ML, Lyonnet S, Amiel J. Heterogeneity of mutationalmechanisms and modes of inheritance in auriculocondylar syndrome. J Med Genet.2013 Mar;50(3):174-86. doi: 10.1136/jmedgenet-2012-101331.
  2. Guion-Almeida ML, Kokitsu-Nakata NM, Zechi-Ceide RM, Vendramini S.Auriculo-condylar syndrome: further evidence for a new disorder. Am J Med Genet. 1999 Sep 10;86(2):130-3.
  3. Guion-Almeida ML, Zechi-Ceide RM, Vendramini S, Kokitsu-Nakata NM.Auriculo-condylar syndrome: additional patients. Am J Med Genet. 2002 Oct1;112(2):209-14.
  4. Masotti C, Oliveira KG, Poerner F, Splendore A, Souza J, Freitas Rda S,Zechi-Ceide R, Guion-Almeida ML, Passos-Bueno MR. Auriculo-condylar syndrome:mapping of a first locus and evidence for genetic heterogeneity. Eur J Hum Genet.2008 Feb;16(2):145-52.
  5. McGowan R, Murday V, Kinning E, Garcia S, Koppel D, Whiteford M. Novelfeatures in auriculo-condylar syndrome. Clin Dysmorphol. 2011 Jan;20(1):1-10.doi: 10.1097/MCD.0b013e32833e56f5.
  6. Rieder MJ, Green GE, Park SS, Stamper BD, Gordon CT, Johnson JM, Cunniff CM,Smith JD, Emery SB, Lyonnet S, Amiel J, Holder M, Heggie AA, Bamshad MJ,Nickerson DA, Cox TC, Hing AV, Horst JA, Cunningham ML. A human homeotictransformation resulting from mutations in PLCB4 and GNAI3 causesauriculocondylar syndrome. Am J Hum Genet. 2012 May 4;90(5):907-14. doi:10.1016/j.ajhg.2012.04.002. Erratum in: Am J Hum Genet. 2012 Aug 10;91(2):397. AmJ Hum Genet. 2012 Jun 8;90(6):1116.
  7. Storm AL, Johnson JM, Lammer E, Green GE, Cunniff C. Auriculo-condylarsyndrome is associated with highly variable ear and mandibular defects inmultiple kindreds. Am J Med Genet A. 2005 Oct 1;138A(2):141-5. Review.
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Update Date: 24 Dec 2020
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