Fetal Nasal Bone Hypoplasia in the Second Trimester as a Marker of Multiple Genetic Syndromes

Nasal bone hypoplasia is associated with a trisomy of chromosome 21, 18 or 13. Nasal bone hypoplasia can also be seen in other, rarer genetic syndromes. The aim of the study was to evaluate the potential of nasal bone hypoplasia, in the second trimester of pregnancy, as a marker of fetal facial dysm...

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Detalles Bibliográficos
Autores principales: Moczulska, Hanna, Serafin, Marcin, Wojda, Katarzyna, Borowiec, Maciej, Sieroszewski, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954562/
https://www.ncbi.nlm.nih.gov/pubmed/35329839
http://dx.doi.org/10.3390/jcm11061513

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954562/
https://www.ncbi.nlm.nih.gov/pubmed/35329839
http://dx.doi.org/10.3390/jcm11061513

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