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Prenatal diagnosis of total arhinia by MRI

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Abstract

Congenital arhinia is the absence of an external nose, nasal cavities and olfactory apparatus, and extremely rare. It occurs during the early gestational stage and may be a result of maldevelopment of the paired nasal placodes embryologically. Total arhinia is often associated with other craniofacial abnormalities. Early detection may be helpful for the parents and physician. However, fewer than 40 patients with arhinia have been reported so far, and most of them were diagnosed after birth. To our knowledge, this is the first case diagnosed by fetal MRI during the second trimester of pregnancy, and confirmed by pathological examination.

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References

  1. Albernaz VS, Castillo M, Mukherji SK, et al. Congenital arhinia. AJNR Am J Neuroradiol. 1996;17:1312–4.

    CAS  PubMed  Google Scholar 

  2. Cusick W, Sullivan CA, Rojas B. Prenatal diagnosis of total arhinia. Ultrasound Obstet Gynecol. 2000;15:259–61.

    Article  CAS  PubMed  Google Scholar 

  3. Majewski S, Donnenfeld AE, Kuhlman K, Patel A. Second-trimester prenatal diagnosis of total arhinia. J Ultrasound Med. 2007;26:391–5.

    PubMed  Google Scholar 

  4. McGlone L. Congenital arhinia. J Ped Child Health. 2003;39:474–6.

    Article  CAS  Google Scholar 

  5. Kazan-Tannus JF, Levine D, McKenzie C, et al. Real-time magnetic resonance imaging aids prenatal diagnosis of isolated cleft palate. J Ultrasound Med. 2005;24:1533–40.

    PubMed  Google Scholar 

  6. Cohen D, Goitein KJ. Arhinia revisted. Rhinology. 1987;25:237–44.

    CAS  PubMed  Google Scholar 

  7. Sato D, Shimokawa O, Harada N, et al. Congenital arhinia: molecular-genetic analysis of five patients. Am J Med Genet A. 2007;143:546–52.

    Article  Google Scholar 

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Correspondence to Xiaobing Li.

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Li, X., Zhang, L. & Wang, F. Prenatal diagnosis of total arhinia by MRI. Jpn J Radiol 33, 672–674 (2015). https://doi.org/10.1007/s11604-015-0473-7

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  • DOI: https://doi.org/10.1007/s11604-015-0473-7

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