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Prenatal Diagnosis of Binder Phenotype, Naso-Maxillar Hypoplasia

Authors :
Pop Lucian Gheorghe
Suciu Ioan Dumitru
Bacalbasa Nicolae
Toader Oana Daniela
Source :
Acta Medica Marisiensis, Vol 66, Iss 4, Pp 160-163 (2020)
Publication Year :
2020
Publisher :
Sciendo, 2020.

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.

Details

Language :
English
ISSN :
22476113
Volume :
66
Issue :
4
Database :
OpenAIRE
Journal :
Acta Medica Marisiensis
Accession number :
edsair.doajarticles..b22277bec689bc9ebcb6ab2bb7a2aad4