<abstract xmlns="http://www.w3.org/1999/xhtml"><p>Facial dysmorphism is a common diagnosis which represents a broad spectrum of aetiologies with different outcomes spreading from normal outcome to foetal demise or new-borns with multiple malformations. Prenatal diagnosis can be difficult, making counselling a challenging task even in experienced hands. This paper aims to present an unusual case of facial dysmorphism (Binder phenotype) which resulted in a normal pregnancy. However, throughout the pregnancy, future parents experienced excruciating anxiety, which required multiple prenatal counselling appointments. We believe that in case of a Binder phenotype, genetic testing, multiple scanning appointments and extensive discussion with future parents are vital in the prevention of an unneeded ending of a pregnancy.</p></abstract>

Facial dysmorphism is a common diagnosis which represents a broad spectrum of aetiologies with different outcomes spreading from normal outcome to foetal demise or new-borns with multiple malformations. Prenatal diagnosis can be difficult, making counselling a challenging task even in experienced hands. This paper aims to present an unusual case of facial dysmorphism (Binder phenotype) which resulted in a normal pregnancy. However, throughout the pregnancy, future parents experienced excruciating anxiety, which required multiple prenatal counselling appointments. We believe that in case of a Binder phenotype, genetic testing, multiple scanning appointments and extensive discussion with future parents are vital in the prevention of an unneeded ending of a pregnancy.

Prenatal Diagnosis of Binder Phenotype, Naso-Maxillar Hypoplasia

University of Medicine and Pharmacy-Carol Davila-

Acta Marisiensis - Seria Medica

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

{"article-title":"Prenatal Diagnosis of Binder Phenotype, Naso-Maxillar Hypoplasia"}

Facial dysmorphism is a common diagnosis which represents a broad spectrum of aetiologies with different outcomes spreading from normal outcome to foetal...

Prenatal Diagnosis of Binder Phenotype, Naso-Maxillar Hypoplasia

Publié en ligne: 31 déc. 2020

Pages: 160 - 163

Reçu: 31 mai 2020

Accepté: 04 nov. 2020

DOI: https://doi.org/10.2478/amma-2020-0032

Mots clés
Binder syndrome, facial anomalies, hypermetropia, anomaly scan

© 2020 Lucian Gheorghe Pop et al., published by Sciendo

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

Prenatal Diagnosis of Binder Phenotype, Naso-Maxillar Hypoplasia

Publié en ligne: 31 déc. 2020

Pages: 160 - 163

Reçu: 31 mai 2020

Accepté: 04 nov. 2020

DOI: https://doi.org/10.2478/amma-2020-0032

Mots clésBinder syndrome, facial anomalies, hypermetropia, anomaly scan

© 2020 Lucian Gheorghe Pop et al., published by Sciendo

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

Mots clés
Binder syndrome, facial anomalies, hypermetropia, anomaly scan