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.
Prenatal Diagnosis of an Extremely Rare Neurological Disease
- Cristina-Crenguta Albu
- Dinu-Florin Albu
Cristina-Crenguta Albu
University of Medicine and Pharmacy “Carol Davila”, Bucharest, Romania 37, Dionisie Lupu Street, 1st District, 020021, Bucharest, Romania Alco San Medical Center, Bucharest, Romania 67, Barbu Vacarescu Bd., 2st District, 020272, Bucharest, Romania
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Dinu-Florin Albu
University of Medicine and Pharmacy “Carol Davila”, Bucharest, Romania 37, Dionisie Lupu Street, 1st District, 020021, Bucharest, Romania Alco San Medical Center, Bucharest, Romania 67, Barbu Vacarescu Bd., 2st District, 020272, Bucharest, Romania
Search for the other articles from the author in:
Google Scholar | PubMed | BMJ Journal
Cite this:
Cristina-Crenguta Albu, & Dinu-Florin Albu. (2019). Prenatal Diagnosis of an Extremely Rare Neurological Disease . Journal of Medical Biomedical and Applied Sciences, 7(12), 300–302. https://doi.org/10.15520/jmbas.v7i12.202
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