Prenatal Diagnosis of an Extremely Rare Neurological Disease
Resumen
We report one clinical case of a 29-year-old, Caucasian woman who is pregnant for the first time. Ultrasound examination showed a singleton fetus with porencephaly. Amniocentesis was done, and the fetal chromosomal analysis revealed a fetus with normal karyotype: 46,XY. After a complex and very difficult genetic counselling the parents opted to terminate the pregnancy. The autopsy confirm the prenatal ultrasound diagnosis.
How to Cite
Cristina-Crenguta Albu, Dinu-Florin Albu (2019). Prenatal Diagnosis of an Extremely Rare Neurological Disease . Journal of Medical Biomedical and Applied Sciences , Vol. 7 Núm. 12 (2019) , 300-302 . https://doi.org/10.15520/jmbas.v7i12.202