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Prenatal Diagnosis of Binder Phenotype, Naso-Maxillar Hypoplasia
- 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.
- Subjects :
- hypermetropia
facial anomalies
binder syndrome
Medicine
anomaly scan
Subjects
Details
- Language :
- English
- ISSN :
- 22476113
- Volume :
- 66
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Acta Medica Marisiensis
- Accession number :
- edsair.doajarticles..b22277bec689bc9ebcb6ab2bb7a2aad4