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Prenatal Binder Phenotype: Physician’s Dilemma-A Case Report

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Journal of Fetal Medicine

Abstract

The Binder phenotype is defined by midface hypoplasia, underdeveloped frontal sinuses, hypoplastic and abnormally positioned nasal bones, nostrils appearing moon or comma-shaped and prognathism. It is heterogeneous in etiology and not fully understood. Multiple causative factors are described. The physician’s dilemma is of diagnosing the fetal abnormalities on antenatal ultrasound for which there is no confirmatory testing. There are management and ethical problems regarding the diagnosis, further investigations and confirmation of the diagnosis. The Binder phenotype is a clinical diagnosis with multiple differential diagnoses. It carries an uncertain and unpredictable course and prognosis which might be difficult for both clinician and parents to predict and comprehend. Genetic counseling has to be variable depending upon the diagnosis.

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References

  1. Chummun S, McLean NR, Nugent M, Anderson PJ, David DJ. Binder syndrome. J CraniofacSurg. 2012;23:986–90.

    Article  Google Scholar 

  2. Binder KH. Dysostosis maxillo-nasalis, ein arhinencephaler Missbildungskomplex. Deutsche Zahnaertzl Z. 1962;17:438.

    Google Scholar 

  3. Keppler-Noreuil KM, Wenzel TJ. Binder phenotype: associated findings and etiologic mechanisms. J CraniofacSurg. 2010;21:1339–45.

    Article  Google Scholar 

  4. Alessandri JL, Ramful D, Cuillier F. Binder phenotype and brachytelephalangic chondrodysplasia punctata secondary to maternal vitamin K deficiency. ClinDysmorphol. 2010;19:85–7.

    Google Scholar 

  5. Demirel G, Oguz SS, Celik IH, Erdeve O, Uras N, Dilmen U. A case of Keutel syndrome diagnosed in the neonatal period: associated with Binder phenotype. Genet Couns. 2012;23:25–30.

    CAS  PubMed  Google Scholar 

  6. Chitayat D, Keating S, Zand DJ, et al. Chondrodysplasia punctata associated with maternal autoimmune diseases: expanding the spectrum from systemic lupus erythematosus (SLE) to mixed connective tissue disease (MCTD) and scleroderma—report of eight cases. Am J Med Genet A. 2008;146A:3038–53.

    Article  Google Scholar 

  7. Levaillant JM, Moeglin D, Zouiten K, et al. Binder phenotype: clinical and etiological heterogeneity of the so-called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature. PrenatDiagn. 2009;29:140–50.

    CAS  Google Scholar 

  8. Lazar DA, Cassady CI, Olutoye OO, et al. Tracheoesophageal displacement index and predictors of airway obstruction for fetuses with neck masses. J PediatrSurg. 2012;47:46–50.

    Google Scholar 

  9. Deshpande SN, Juneja MH. Binder’s syndrome (maxillonasal dysplasia) different treatment modalities: our experience. Indian J PlastSurg. 2012;45:62–6.

    Google Scholar 

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Correspondence to Ashutosh Gupta.

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Gupta, A., Aneja, A., Bahl, N. et al. Prenatal Binder Phenotype: Physician’s Dilemma-A Case Report. J. Fetal Med. 8, 65–70 (2021). https://doi.org/10.1007/s40556-020-00283-2

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  • DOI: https://doi.org/10.1007/s40556-020-00283-2

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